Canonical Allele Identifier: CA1846866629

Gene: GRHPR

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37426639T= , CM000671.2:g.37426639T=	GRCh38
NC_000009.11:g.37426636T= , CM000671.1:g.37426636T=	GRCh37
NC_000009.10:g.37416636T=	NCBI36
NG_008135.1:g.8930T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000318158.11:c.389T= MANE Select	ENSP00000313432.6:p.Ile130=
ENST00000318158.10:c.389T=	ENSP00000313432.6:p.Ile130=
ENST00000377824.8:n.426T=
ENST00000460882.5:n.416T=
ENST00000487399.5:n.941T=
ENST00000491488.5:n.110-1845T=
ENST00000493368.5:n.446T=
ENST00000607784.1:c.389T=	ENSP00000475569.1:p.Ile130=
NM_012203.1:c.389T=	NP_036335.1:p.Ile130=
XM_005251631.1:c.84-1845T=	XP_005251688.1:n.84-1845T=
XM_011518073.1:c.-374T=	XP_011516375.1:n.-374T=
XR_929374.1:n.474T=
XM_017015320.2:c.389T=	XP_016870809.1:p.Ile130=
XM_017015321.2:c.389T=	XP_016870810.1:p.Ile130=
XM_017015323.2:c.-374T=	XP_016870812.1:n.-374T=
XM_024447716.1:c.662T=	XP_024303484.1:p.Ile221=
XM_024447717.1:c.662T=	XP_024303485.1:p.Ile221=
XR_002956828.1:n.677T=
XR_002956829.1:n.677T=
XR_002956830.1:n.448T=
XR_002956831.1:n.139-1845T=
XR_002956832.1:n.448T=
NM_012203.2:c.389T= MANE Select	NP_036335.1:p.Ile130=