Canonical Allele Identifier: CA1846869141

Gene: GRHPR

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37428565G= , CM000671.2:g.37428565G=	GRCh38
NC_000009.11:g.37428562G= , CM000671.1:g.37428562G=	GRCh37
NC_000009.10:g.37418562G=	NCBI36
NG_008135.1:g.10856G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318158.11:c.486G= MANE Select	ENSP00000313432.6:p.Gly162=
ENST00000318158.10:c.486G=	ENSP00000313432.6:p.Gly162=
ENST00000377824.8:n.523G=
ENST00000460882.5:n.513G=
ENST00000480596.5:n.28G=
ENST00000491488.5:n.191G=
ENST00000493368.5:n.543G=
ENST00000497693.1:n.860G=
ENST00000607784.1:c.486G=	ENSP00000475569.1:p.Gly162=
NM_012203.1:c.486G=	NP_036335.1:p.Gly162=
XM_005251631.1:c.165G=	XP_005251688.1:p.Gly55=
XM_011518073.1:c.-277G=	XP_011516375.1:n.-277G=
XR_929374.1:n.571G=
XM_017015320.2:c.486G=	XP_016870809.1:p.Gly162=
XM_017015321.2:c.486G=	XP_016870810.1:p.Gly162=
XM_017015323.2:c.-277G=	XP_016870812.1:n.-277G=
XM_024447716.1:c.759G=	XP_024303484.1:p.Gly253=
XM_024447717.1:c.759G=	XP_024303485.1:p.Gly253=
XR_002956828.1:n.774G=
XR_002956829.1:n.774G=
XR_002956830.1:n.545G=
XR_002956831.1:n.220G=
XR_002956832.1:n.545G=
NM_012203.2:c.486G= MANE Select	NP_036335.1:p.Gly162=