Canonical Allele Identifier: CA1846869125

Gene: GRHPR

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37428557G= , CM000671.2:g.37428557G=	GRCh38
NC_000009.11:g.37428554G= , CM000671.1:g.37428554G=	GRCh37
NC_000009.10:g.37418554G=	NCBI36
NG_008135.1:g.10848G=

Transcript Alleles

HGVS	Amino-acid Change
NM_012203.2:c.478G= MANE Select	NP_036335.1:p.Gly160=
ENST00000318158.11:c.478G= MANE Select	ENSP00000313432.6:p.Gly160=
NM_012203.1:c.478G=	NP_036335.1:p.Gly160=
ENST00000318158.10:c.478G=	ENSP00000313432.6:p.Gly160=
ENST00000377824.8:n.515G=
ENST00000460882.5:n.505G=
ENST00000480596.5:n.20G=
ENST00000491488.5:n.183G=
ENST00000493368.5:n.535G=
ENST00000497693.1:n.852G=
ENST00000607784.1:c.478G=	ENSP00000475569.1:p.Gly160=
XM_005251631.1:c.157G=	XP_005251688.1:p.Gly53=
XM_011518073.1:c.-285G=	XP_011516375.1:n.-285G=
XM_017015320.2:c.478G=	XP_016870809.1:p.Gly160=
XM_017015321.2:c.478G=	XP_016870810.1:p.Gly160=
XM_017015323.2:c.-285G=	XP_016870812.1:n.-285G=
XM_024447716.1:c.751G=	XP_024303484.1:p.Gly251=
XM_024447717.1:c.751G=	XP_024303485.1:p.Gly251=
XR_002956828.1:n.766G=
XR_002956829.1:n.766G=
XR_002956830.1:n.537G=
XR_002956831.1:n.212G=
XR_002956832.1:n.537G=
XR_929374.1:n.563G=