Canonical Allele Identifier: CA1846870471

Gene: GRHPR

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37429746C= , CM000671.2:g.37429746C=	GRCh38
NC_000009.11:g.37429743C= , CM000671.1:g.37429743C=	GRCh37
NC_000009.10:g.37419743C=	NCBI36
NG_008135.1:g.12037C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318158.11:c.508C= MANE Select	ENSP00000313432.6:p.Arg170=
ENST00000318158.10:c.508C=	ENSP00000313432.6:p.Arg170=
ENST00000377824.8:n.545C=
ENST00000460882.5:n.535C=
ENST00000480596.5:n.1209C=
ENST00000491488.5:n.213C=
ENST00000494290.1:c.79C=	ENSP00000432021.1:p.Arg27=
ENST00000497693.1:n.2041C=
ENST00000607784.1:c.508C=	ENSP00000475569.1:p.Arg170=
NM_012203.1:c.508C=	NP_036335.1:p.Arg170=
XM_005251631.1:c.187C=	XP_005251688.1:p.Arg63=
XM_011518073.1:c.106C=	XP_011516375.1:p.Arg36=
XR_929374.1:n.953C=
XM_017015320.2:c.508C=	XP_016870809.1:p.Arg170=
XM_017015321.2:c.508C=	XP_016870810.1:p.Arg170=
XM_017015323.2:c.106C=	XP_016870812.1:p.Arg36=
XM_024447716.1:c.781C=	XP_024303484.1:p.Arg261=
XM_024447717.1:c.781C=	XP_024303485.1:p.Arg261=
XR_002956828.1:n.796C=
XR_002956829.1:n.796C=
XR_002956830.1:n.567C=
XR_002956831.1:n.242C=
XR_002956832.1:n.927C=
NM_012203.2:c.508C= MANE Select	NP_036335.1:p.Arg170=