Canonical Allele Identifier: CA373443317
Gene: GRHPR HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.37429762T>A , CM000671.2:g.37429762T>A GRCh38
NC_000009.11:g.37429759T>A , CM000671.1:g.37429759T>A GRCh37
NC_000009.10:g.37419759T>A NCBI36
NG_008135.1:g.12053T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000318158.11:c.524T>A MANE Select ENSP00000313432.6:p.Phe175Tyr
ENST00000318158.10:c.524T>A ENSP00000313432.6:p.Phe175Tyr
ENST00000377824.8:n.561T>A
ENST00000460882.5:n.551T>A
ENST00000480596.5:n.1225T>A
ENST00000491488.5:n.229T>A
ENST00000494290.1:c.95T>A ENSP00000432021.1:p.Phe32Tyr
ENST00000497693.1:n.2057T>A
ENST00000607784.1:c.524T>A ENSP00000475569.1:p.Phe175Tyr
NM_012203.1:c.524T>A NP_036335.1:p.Phe175Tyr
XM_005251631.1:c.203T>A XP_005251688.1:p.Phe68Tyr
XM_011518073.1:c.122T>A XP_011516375.1:p.Phe41Tyr
XR_929374.1:n.969T>A
XM_017015320.2:c.524T>A XP_016870809.1:p.Phe175Tyr
XM_017015321.2:c.524T>A XP_016870810.1:p.Phe175Tyr
XM_017015323.2:c.122T>A XP_016870812.1:p.Phe41Tyr
XM_024447716.1:c.797T>A XP_024303484.1:p.Phe266Tyr
XM_024447717.1:c.797T>A XP_024303485.1:p.Phe266Tyr
XR_002956828.1:n.812T>A
XR_002956829.1:n.812T>A
XR_002956830.1:n.583T>A
XR_002956831.1:n.258T>A
XR_002956832.1:n.943T>A
NM_012203.2:c.524T>A MANE Select NP_036335.1:p.Phe175Tyr