Canonical Allele Identifier: CA1846865826

Gene: GRHPR

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37425994G= , CM000671.2:g.37425994G=	GRCh38
NC_000009.11:g.37425991G= , CM000671.1:g.37425991G=	GRCh37
NC_000009.10:g.37415991G=	NCBI36
NG_008135.1:g.8285G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318158.11:c.287G= MANE Select	ENSP00000313432.6:p.Arg96=
ENST00000318158.10:c.287G=	ENSP00000313432.6:p.Arg96=
ENST00000377824.8:n.324G=
ENST00000460882.5:n.314G=
ENST00000487399.5:n.296G=
ENST00000491488.5:n.110-2490G=
ENST00000493368.5:n.344G=
ENST00000607784.1:c.287G=	ENSP00000475569.1:p.Arg96=
NM_012203.1:c.287G=	NP_036335.1:p.Arg96=
XM_005251631.1:c.84-2490G=	XP_005251688.1:n.84-2490G=
XM_011518073.1:c.-476G=	XP_011516375.1:n.-476G=
XR_929374.1:n.372G=
XM_017015320.2:c.287G=	XP_016870809.1:p.Arg96=
XM_017015321.2:c.287G=	XP_016870810.1:p.Arg96=
XM_017015323.2:c.-476G=	XP_016870812.1:n.-476G=
XM_024447716.1:c.560G=	XP_024303484.1:p.Arg187=
XM_024447717.1:c.560G=	XP_024303485.1:p.Arg187=
XR_002956828.1:n.575G=
XR_002956829.1:n.575G=
XR_002956830.1:n.346G=
XR_002956831.1:n.139-2490G=
XR_002956832.1:n.346G=
NM_012203.2:c.287G= MANE Select	NP_036335.1:p.Arg96=