Canonical Allele Identifier: CA1846866650

Gene: GRHPR

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37426648T= , CM000671.2:g.37426648T=	GRCh38
NC_000009.11:g.37426645T= , CM000671.1:g.37426645T=	GRCh37
NC_000009.10:g.37416645T=	NCBI36
NG_008135.1:g.8939T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318158.11:c.398T= MANE Select	ENSP00000313432.6:p.Val133=
ENST00000318158.10:c.398T=	ENSP00000313432.6:p.Val133=
ENST00000377824.8:n.435T=
ENST00000460882.5:n.425T=
ENST00000487399.5:n.950T=
ENST00000491488.5:n.110-1836T=
ENST00000493368.5:n.455T=
ENST00000607784.1:c.398T=	ENSP00000475569.1:p.Val133=
NM_012203.1:c.398T=	NP_036335.1:p.Val133=
XM_005251631.1:c.84-1836T=	XP_005251688.1:n.84-1836T=
XM_011518073.1:c.-365T=	XP_011516375.1:n.-365T=
XR_929374.1:n.483T=
XM_017015320.2:c.398T=	XP_016870809.1:p.Val133=
XM_017015321.2:c.398T=	XP_016870810.1:p.Val133=
XM_017015323.2:c.-365T=	XP_016870812.1:n.-365T=
XM_024447716.1:c.671T=	XP_024303484.1:p.Val224=
XM_024447717.1:c.671T=	XP_024303485.1:p.Val224=
XR_002956828.1:n.686T=
XR_002956829.1:n.686T=
XR_002956830.1:n.457T=
XR_002956831.1:n.139-1836T=
XR_002956832.1:n.457T=
NM_012203.2:c.398T= MANE Select	NP_036335.1:p.Val133=