Canonical Allele Identifier: CA1846873985

Gene: GRHPR

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37432027G= , CM000671.2:g.37432027G=	GRCh38
NC_000009.11:g.37432024G= , CM000671.1:g.37432024G=	GRCh37
NC_000009.10:g.37422024G=	NCBI36
NG_008135.1:g.14318G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000318158.11:c.754G= MANE Select	ENSP00000313432.6:p.Asp252=
ENST00000318158.10:c.754G=	ENSP00000313432.6:p.Asp252=
ENST00000460882.5:n.781G=
ENST00000480596.5:n.1455G=
ENST00000482603.1:n.207G=
ENST00000491488.5:n.459G=
ENST00000494290.1:c.*51+876G=	ENSP00000432021.1:n.*51+876G=
ENST00000497693.1:n.4322G=
ENST00000607784.1:c.754G=	ENSP00000475569.1:p.Asp252=
NM_012203.1:c.754G=	NP_036335.1:p.Asp252=
XM_005251631.1:c.433G=	XP_005251688.1:p.Asp145=
XM_011518073.1:c.352G=	XP_011516375.1:p.Asp118=
XM_017015320.2:c.754G=	XP_016870809.1:p.Asp252=
XM_017015321.2:c.754G=	XP_016870810.1:p.Asp252=
XM_017015323.2:c.352G=	XP_016870812.1:p.Asp118=
XM_024447716.1:c.1027G=	XP_024303484.1:p.Asp343=
XM_024447717.1:c.1027G=	XP_024303485.1:p.Asp343=
XR_002956828.1:n.1042G=
XR_002956829.1:n.1042G=
XR_002956830.1:n.2174G=
XR_002956831.1:n.1849G=
XR_002956832.1:n.1173G=
NM_012203.2:c.754G= MANE Select	NP_036335.1:p.Asp252=