Canonical Allele Identifier: CA1846869077

Gene: GRHPR

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37428536C= , CM000671.2:g.37428536C=	GRCh38
NC_000009.11:g.37428533C= , CM000671.1:g.37428533C=	GRCh37
NC_000009.10:g.37418533C=	NCBI36
NG_008135.1:g.10827C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318158.11:c.457C= MANE Select	ENSP00000313432.6:p.Gln153=
ENST00000318158.10:c.457C=	ENSP00000313432.6:p.Gln153=
ENST00000377824.8:n.494C=
ENST00000460882.5:n.484C=
ENST00000491488.5:n.162C=
ENST00000493368.5:n.514C=
ENST00000497693.1:n.831C=
ENST00000607784.1:c.457C=	ENSP00000475569.1:p.Gln153=
NM_012203.1:c.457C=	NP_036335.1:p.Gln153=
XM_005251631.1:c.136C=	XP_005251688.1:p.Gln46=
XM_011518073.1:c.-306C=	XP_011516375.1:n.-306C=
XR_929374.1:n.542C=
XM_017015320.2:c.457C=	XP_016870809.1:p.Gln153=
XM_017015321.2:c.457C=	XP_016870810.1:p.Gln153=
XM_017015323.2:c.-306C=	XP_016870812.1:n.-306C=
XM_024447716.1:c.730C=	XP_024303484.1:p.Gln244=
XM_024447717.1:c.730C=	XP_024303485.1:p.Gln244=
XR_002956828.1:n.745C=
XR_002956829.1:n.745C=
XR_002956830.1:n.516C=
XR_002956831.1:n.191C=
XR_002956832.1:n.516C=
NM_012203.2:c.457C= MANE Select	NP_036335.1:p.Gln153=