Canonical Allele Identifier: CA10794905
Gene: RGS7 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.240824454C>T , CM000663.2:g.240824454C>T GRCh38
NC_000001.10:g.240987754C>T , CM000663.1:g.240987754C>T GRCh37
NC_000001.9:g.239054377C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000685354.1:n.1210+2644G>A
ENST00000685936.1:c.606+2644G>A ENSP00000510372.1:n.606+2644G>A
ENST00000686049.1:n.803+2644G>A
ENST00000686241.1:n.764+2644G>A
ENST00000686277.1:n.562+2644G>A
ENST00000686340.1:c.*584+2644G>A ENSP00000508697.1:n.*584+2644G>A
ENST00000686465.1:c.606+2644G>A ENSP00000508545.1:n.606+2644G>A
ENST00000686645.1:n.524+2644G>A
ENST00000686908.1:c.682-8039G>A ENSP00000510420.1:n.682-8039G>A
ENST00000687018.1:c.*593+2644G>A ENSP00000509943.1:n.*593+2644G>A
ENST00000687040.1:c.*130+2644G>A ENSP00000509260.1:n.*130+2644G>A
ENST00000687448.1:c.606+2644G>A ENSP00000510187.1:n.606+2644G>A
ENST00000687793.1:n.600+2644G>A
ENST00000687918.1:n.712+2644G>A
ENST00000687977.1:n.1210+2644G>A
ENST00000688216.1:n.650+2644G>A
ENST00000688438.1:n.759+2644G>A
ENST00000688545.1:c.*52+2644G>A ENSP00000509302.1:n.*52+2644G>A
ENST00000688633.1:c.756+2644G>A ENSP00000509822.1:n.756+2644G>A
ENST00000688703.1:c.606+2644G>A ENSP00000510116.1:n.606+2644G>A
ENST00000688737.1:c.684+2644G>A ENSP00000510154.1:n.684+2644G>A
ENST00000688738.1:n.395+2644G>A
ENST00000688863.1:c.684+2644G>A ENSP00000509381.1:n.684+2644G>A
ENST00000689115.1:c.525+2644G>A ENSP00000510458.1:n.525+2644G>A
ENST00000689223.1:n.680+2644G>A
ENST00000689602.1:c.606+2644G>A ENSP00000510103.1:n.606+2644G>A
ENST00000689639.1:n.746+2644G>A
ENST00000689640.1:c.408+2644G>A ENSP00000510326.1:n.408+2644G>A
ENST00000690019.1:c.633+2644G>A ENSP00000510735.1:n.633+2644G>A
ENST00000690224.1:n.733+2644G>A
ENST00000690236.1:n.723+2644G>A
ENST00000690356.1:c.*238+2644G>A ENSP00000509411.1:n.*238+2644G>A
ENST00000690539.1:c.684+2644G>A ENSP00000510322.1:n.684+2644G>A
ENST00000690614.1:c.606+2644G>A ENSP00000509835.1:n.606+2644G>A
ENST00000691271.1:n.1210+2644G>A
ENST00000691285.1:n.602+2644G>A
ENST00000691399.1:n.1004+2644G>A
ENST00000691485.1:c.606+2644G>A ENSP00000509318.1:n.606+2644G>A
ENST00000691597.1:n.1856+2644G>A
ENST00000691979.1:c.684+2644G>A ENSP00000510676.1:n.684+2644G>A
ENST00000691989.1:c.684+2644G>A ENSP00000508919.1:n.684+2644G>A
ENST00000692410.1:c.606+2644G>A ENSP00000509046.1:n.606+2644G>A
ENST00000692860.1:n.1210+2644G>A
ENST00000693043.1:c.525+2644G>A ENSP00000508520.1:n.525+2644G>A
ENST00000693448.1:n.680+2644G>A
ENST00000440928.6:c.684+2644G>A MANE Select ENSP00000404399.2:n.684+2644G>A
ENST00000348120.6:c.525+2644G>A ENSP00000341242.2:n.525+2644G>A
ENST00000366562.8:c.432+2644G>A ENSP00000355520.5:n.432+2644G>A
ENST00000366563.5:c.684+2644G>A ENSP00000355521.1:n.684+2644G>A
ENST00000366564.5:c.684+2644G>A ENSP00000355522.1:n.684+2644G>A
ENST00000366565.5:c.684+2644G>A ENSP00000355523.1:n.684+2644G>A
ENST00000401882.2:c.447+2644G>A ENSP00000385508.2:n.447+2644G>A
ENST00000440928.5:c.177+2644G>A ENSP00000404399.1:n.177+2644G>A
ENST00000446183.6:c.432+2644G>A ENSP00000390138.2:n.432+2644G>A
NM_001282773.1:c.525+2644G>A NP_001269702.1:n.525+2644G>A
NM_001282775.1:c.684+2644G>A NP_001269704.1:n.684+2644G>A
NM_001282778.1:c.684+2644G>A NP_001269707.1:n.684+2644G>A
NM_002924.5:c.684+2644G>A NP_002915.3:n.684+2644G>A
XM_005273218.2:c.684+2644G>A XP_005273275.1:n.684+2644G>A
XM_005273221.3:c.606+2644G>A XP_005273278.1:n.606+2644G>A
XM_006711800.2:c.606+2644G>A XP_006711863.1:n.606+2644G>A
XM_011544246.1:c.606+2644G>A XP_011542548.1:n.606+2644G>A
XM_011544247.1:c.606+2644G>A XP_011542549.1:n.606+2644G>A
XR_949321.1:n.39-448C>T
XR_949322.1:n.39-448C>T
NM_001282773.2:c.525+2644G>A NP_001269702.1:n.525+2644G>A
NM_001282775.2:c.684+2644G>A NP_001269704.1:n.684+2644G>A
NM_001282778.2:c.684+2644G>A NP_001269707.1:n.684+2644G>A
NM_001350113.1:c.606+2644G>A NP_001337042.1:n.606+2644G>A
NM_001350114.1:c.606+2644G>A NP_001337043.1:n.606+2644G>A
NM_001350115.1:c.606+2644G>A NP_001337044.1:n.606+2644G>A
NM_001350116.1:c.606+2644G>A NP_001337045.1:n.606+2644G>A
NM_001364886.1:c.684+2644G>A MANE Select NP_001351815.1:n.684+2644G>A
NM_002924.6:c.684+2644G>A NP_002915.3:n.684+2644G>A
XM_006711800.4:c.606+2644G>A XP_006711863.1:n.606+2644G>A
XM_011544246.3:c.606+2644G>A XP_011542548.1:n.606+2644G>A
XM_011544247.3:c.606+2644G>A XP_011542549.1:n.606+2644G>A
XM_017002001.2:c.633+2644G>A XP_016857490.1:n.633+2644G>A
XM_017002002.2:c.606+2644G>A XP_016857491.1:n.606+2644G>A
XM_017002003.2:c.633+2644G>A XP_016857492.1:n.633+2644G>A
XM_017002004.2:c.633+2644G>A XP_016857493.1:n.633+2644G>A
XM_017002005.2:c.606+2644G>A XP_016857494.1:n.606+2644G>A
XM_017002009.1:c.606+2644G>A XP_016857498.1:n.606+2644G>A
XM_017002011.2:c.432+2644G>A XP_016857500.1:n.432+2644G>A
XM_017002012.2:c.432+2644G>A XP_016857501.1:n.432+2644G>A
XM_017002013.1:c.432+2644G>A XP_016857502.1:n.432+2644G>A
NM_001374806.1:c.633+2644G>A NP_001361735.1:n.633+2644G>A
NM_001374807.1:c.633+2644G>A NP_001361736.1:n.633+2644G>A
NM_001374808.1:c.606+2644G>A NP_001361737.1:n.606+2644G>A
NM_001374809.1:c.405+2644G>A NP_001361738.1:n.405+2644G>A
NM_001374810.1:c.405+2644G>A NP_001361739.1:n.405+2644G>A
NM_001374811.1:c.525+2644G>A NP_001361740.1:n.525+2644G>A
NM_001374812.1:c.610-8039G>A NP_001361741.1:n.610-8039G>A
NM_001374813.1:c.171+2644G>A NP_001361742.1:n.171+2644G>A
NM_001374814.1:c.525+2644G>A NP_001361743.1:n.525+2644G>A
NM_001374815.1:c.684+2644G>A NP_001361744.1:n.684+2644G>A
NM_001374816.1:c.684+2644G>A NP_001361745.1:n.684+2644G>A
NM_001350113.2:c.606+2644G>A NP_001337042.1:n.606+2644G>A
NM_001350114.2:c.606+2644G>A NP_001337043.1:n.606+2644G>A
NM_001350115.2:c.606+2644G>A NP_001337044.1:n.606+2644G>A
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