Canonical Allele Identifier: CA1846885960

Gene: GRHPR

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37436761G= , CM000671.2:g.37436761G=	GRCh38
NC_000009.11:g.37436758G= , CM000671.1:g.37436758G=	GRCh37
NC_000009.10:g.37426758G=	NCBI36
NG_008135.1:g.19052G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318158.11:c.966G= MANE Select	ENSP00000313432.6:p.Met322=
ENST00000318158.10:c.966G=	ENSP00000313432.6:p.Met322=
ENST00000460882.5:n.993G=
ENST00000480596.5:n.1667G=
ENST00000494290.1:c.*52-120G=	ENSP00000432021.1:n.*52-120G=
ENST00000497693.1:n.4534G=
NM_012203.1:c.966G=	NP_036335.1:p.Met322=
XM_005251631.1:c.645G=	XP_005251688.1:p.Met215=
XM_011518073.1:c.564G=	XP_011516375.1:p.Met188=
XM_017015320.2:c.946-650G=	XP_016870809.1:n.946-650G=
XM_017015321.2:c.866-650G=	XP_016870810.1:n.866-650G=
XM_017015323.2:c.544-650G=	XP_016870812.1:n.544-650G=
XM_024447716.1:c.1219-650G=	XP_024303484.1:n.1219-650G=
XM_024447717.1:c.1139-650G=	XP_024303485.1:n.1139-650G=
XR_002956828.1:n.1234-650G=
XR_002956829.1:n.1154-650G=
XR_002956830.1:n.2386G=
XR_002956831.1:n.2061G=
XR_002956832.1:n.1385G=
NM_012203.2:c.966G= MANE Select	NP_036335.1:p.Met322=