Canonical Allele Identifier: CA1846886761

Gene: GRHPR

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37436858T= , CM000671.2:g.37436858T=	GRCh38
NC_000009.11:g.37436855T= , CM000671.1:g.37436855T=	GRCh37
NC_000009.10:g.37426855T=	NCBI36
NG_008135.1:g.19149T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318158.11:c.*76T= MANE Select	ENSP00000313432.6:n.*76T=
ENST00000318158.10:c.*76T=	ENSP00000313432.6:n.*76T=
ENST00000480596.5:n.1764T=
ENST00000494290.1:c.*52-23T=	ENSP00000432021.1:n.*52-23T=
ENST00000497693.1:n.4631T=
NM_012203.1:c.*76T=	NP_036335.1:n.*76T=
XM_005251631.1:c.*76T=	XP_005251688.1:n.*76T=
XM_011518073.1:c.*76T=	XP_011516375.1:n.*76T=
XM_017015320.2:c.946-553T=	XP_016870809.1:n.946-553T=
XM_017015321.2:c.866-553T=	XP_016870810.1:n.866-553T=
XM_017015323.2:c.544-553T=	XP_016870812.1:n.544-553T=
XM_024447716.1:c.1219-553T=	XP_024303484.1:n.1219-553T=
XM_024447717.1:c.1139-553T=	XP_024303485.1:n.1139-553T=
XR_002956828.1:n.1234-553T=
XR_002956829.1:n.1154-553T=
XR_002956830.1:n.2483T=
XR_002956831.1:n.2158T=
XR_002956832.1:n.1482T=
NM_012203.2:c.*76T= MANE Select	NP_036335.1:n.*76T=