Canonical Allele Identifier: CA1846866314
Gene: GRHPR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.37426535T= , CM000671.2:g.37426535T= GRCh38
NC_000009.11:g.37426532T= , CM000671.1:g.37426532T= GRCh37
NC_000009.10:g.37416532T= NCBI36
NG_008135.1:g.8826T=

Transcript Alleles

HGVS Amino-acid change
ENST00000318158.11:c.288-3T= MANE Select ENSP00000313432.6:n.288-3T=
ENST00000318158.10:c.288-3T= ENSP00000313432.6:n.288-3T=
ENST00000377824.8:n.325-3T=
ENST00000460882.5:n.315-3T=
ENST00000487399.5:n.837T=
ENST00000491488.5:n.110-1949T=
ENST00000493368.5:n.345-3T=
ENST00000607784.1:c.288-3T= ENSP00000475569.1:n.288-3T=
NM_012203.1:c.288-3T= NP_036335.1:n.288-3T=
XM_005251631.1:c.84-1949T= XP_005251688.1:n.84-1949T=
XM_011518073.1:c.-475-3T= XP_011516375.1:n.-475-3T=
XR_929374.1:n.373-3T=
XM_017015320.2:c.288-3T= XP_016870809.1:n.288-3T=
XM_017015321.2:c.288-3T= XP_016870810.1:n.288-3T=
XM_017015323.2:c.-475-3T= XP_016870812.1:n.-475-3T=
XM_024447716.1:c.561-3T= XP_024303484.1:n.561-3T=
XM_024447717.1:c.561-3T= XP_024303485.1:n.561-3T=
XR_002956828.1:n.576-3T=
XR_002956829.1:n.576-3T=
XR_002956830.1:n.347-3T=
XR_002956831.1:n.139-1949T=
XR_002956832.1:n.347-3T=
NM_012203.2:c.288-3T= MANE Select NP_036335.1:n.288-3T=