Canonical Allele Identifier: CA1846885969

Gene: GRHPR

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37436762C= , CM000671.2:g.37436762C=	GRCh38
NC_000009.11:g.37436759C= , CM000671.1:g.37436759C=	GRCh37
NC_000009.10:g.37426759C=	NCBI36
NG_008135.1:g.19053C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318158.11:c.967C= MANE Select	ENSP00000313432.6:p.Pro323=
ENST00000318158.10:c.967C=	ENSP00000313432.6:p.Pro323=
ENST00000460882.5:n.994C=
ENST00000480596.5:n.1668C=
ENST00000494290.1:c.*52-119C=	ENSP00000432021.1:n.*52-119C=
ENST00000497693.1:n.4535C=
NM_012203.1:c.967C=	NP_036335.1:p.Pro323=
XM_005251631.1:c.646C=	XP_005251688.1:p.Pro216=
XM_011518073.1:c.565C=	XP_011516375.1:p.Pro189=
XM_017015320.2:c.946-649C=	XP_016870809.1:n.946-649C=
XM_017015321.2:c.866-649C=	XP_016870810.1:n.866-649C=
XM_017015323.2:c.544-649C=	XP_016870812.1:n.544-649C=
XM_024447716.1:c.1219-649C=	XP_024303484.1:n.1219-649C=
XM_024447717.1:c.1139-649C=	XP_024303485.1:n.1139-649C=
XR_002956828.1:n.1234-649C=
XR_002956829.1:n.1154-649C=
XR_002956830.1:n.2387C=
XR_002956831.1:n.2062C=
XR_002956832.1:n.1386C=
NM_012203.2:c.967C= MANE Select	NP_036335.1:p.Pro323=