Canonical Allele Identifier: CA1846885475
Gene: GRHPR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.37436649T= , CM000671.2:g.37436649T= GRCh38
NC_000009.11:g.37436646T= , CM000671.1:g.37436646T= GRCh37
NC_000009.10:g.37426646T= NCBI36
NG_008135.1:g.18940T=

Transcript Alleles

HGVS Amino-acid change
ENST00000318158.11:c.866-12T= MANE Select ENSP00000313432.6:n.866-12T=
ENST00000318158.10:c.866-12T= ENSP00000313432.6:n.866-12T=
ENST00000460882.5:n.893-12T=
ENST00000480596.5:n.1567-12T=
ENST00000491488.5:n.571-12T=
ENST00000494290.1:c.*52-232T= ENSP00000432021.1:n.*52-232T=
ENST00000497693.1:n.4434-12T=
NM_012203.1:c.866-12T= NP_036335.1:n.866-12T=
XM_005251631.1:c.545-12T= XP_005251688.1:n.545-12T=
XM_011518073.1:c.464-12T= XP_011516375.1:n.464-12T=
XM_017015320.2:c.946-762T= XP_016870809.1:n.946-762T=
XM_017015321.2:c.866-762T= XP_016870810.1:n.866-762T=
XM_017015323.2:c.544-762T= XP_016870812.1:n.544-762T=
XM_024447716.1:c.1219-762T= XP_024303484.1:n.1219-762T=
XM_024447717.1:c.1139-762T= XP_024303485.1:n.1139-762T=
XR_002956828.1:n.1234-762T=
XR_002956829.1:n.1154-762T=
XR_002956830.1:n.2286-12T=
XR_002956831.1:n.1961-12T=
XR_002956832.1:n.1285-12T=
NM_012203.2:c.866-12T= MANE Select NP_036335.1:n.866-12T=