Canonical Allele Identifier: CA1846866379
Gene: GRHPR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.37426556C= , CM000671.2:g.37426556C= GRCh38
NC_000009.11:g.37426553C= , CM000671.1:g.37426553C= GRCh37
NC_000009.10:g.37416553C= NCBI36
NG_008135.1:g.8847C=

Transcript Alleles

HGVS Amino-acid change
ENST00000318158.11:c.306C= MANE Select ENSP00000313432.6:p.Tyr102=
ENST00000318158.10:c.306C= ENSP00000313432.6:p.Tyr102=
ENST00000377824.8:n.343C=
ENST00000460882.5:n.333C=
ENST00000487399.5:n.858C=
ENST00000491488.5:n.110-1928C=
ENST00000493368.5:n.363C=
ENST00000607784.1:c.306C= ENSP00000475569.1:p.Tyr102=
NM_012203.1:c.306C= NP_036335.1:p.Tyr102=
XM_005251631.1:c.84-1928C= XP_005251688.1:n.84-1928C=
XM_011518073.1:c.-457C= XP_011516375.1:n.-457C=
XR_929374.1:n.391C=
XM_017015320.2:c.306C= XP_016870809.1:p.Tyr102=
XM_017015321.2:c.306C= XP_016870810.1:p.Tyr102=
XM_017015323.2:c.-457C= XP_016870812.1:n.-457C=
XM_024447716.1:c.579C= XP_024303484.1:p.Tyr193=
XM_024447717.1:c.579C= XP_024303485.1:p.Tyr193=
XR_002956828.1:n.594C=
XR_002956829.1:n.594C=
XR_002956830.1:n.365C=
XR_002956831.1:n.139-1928C=
XR_002956832.1:n.365C=
NM_012203.2:c.306C= MANE Select NP_036335.1:p.Tyr102=