Canonical Allele Identifier: CA1846870271
Gene: GRHPR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.37429626T= , CM000671.2:g.37429626T= GRCh38
NC_000009.11:g.37429623T= , CM000671.1:g.37429623T= GRCh37
NC_000009.10:g.37419623T= NCBI36
NG_008135.1:g.11917T=

Transcript Alleles

HGVS Amino-acid change
ENST00000318158.11:c.494-106T= MANE Select ENSP00000313432.6:n.494-106T=
ENST00000318158.10:c.494-106T= ENSP00000313432.6:n.494-106T=
ENST00000377824.8:n.531-106T=
ENST00000460882.5:n.521-106T=
ENST00000480596.5:n.1089T=
ENST00000491488.5:n.199-106T=
ENST00000494290.1:c.-42T= ENSP00000432021.1:n.-42T=
ENST00000497693.1:n.1921T=
ENST00000607784.1:c.494-106T= ENSP00000475569.1:n.494-106T=
NM_012203.1:c.494-106T= NP_036335.1:n.494-106T=
XM_005251631.1:c.173-106T= XP_005251688.1:n.173-106T=
XM_011518073.1:c.92-106T= XP_011516375.1:n.92-106T=
XR_929374.1:n.939-106T=
XM_017015320.2:c.494-106T= XP_016870809.1:n.494-106T=
XM_017015321.2:c.494-106T= XP_016870810.1:n.494-106T=
XM_017015323.2:c.92-106T= XP_016870812.1:n.92-106T=
XM_024447716.1:c.767-106T= XP_024303484.1:n.767-106T=
XM_024447717.1:c.767-106T= XP_024303485.1:n.767-106T=
XR_002956828.1:n.782-106T=
XR_002956829.1:n.782-106T=
XR_002956830.1:n.553-106T=
XR_002956831.1:n.228-106T=
XR_002956832.1:n.913-106T=
NM_012203.2:c.494-106T= MANE Select NP_036335.1:n.494-106T=