Canonical Allele Identifier: CA1846870466

Gene: GRHPR

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37429744C= , CM000671.2:g.37429744C=	GRCh38
NC_000009.11:g.37429741C= , CM000671.1:g.37429741C=	GRCh37
NC_000009.10:g.37419741C=	NCBI36
NG_008135.1:g.12035C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000318158.11:c.506C= MANE Select	ENSP00000313432.6:p.Ala169=
ENST00000318158.10:c.506C=	ENSP00000313432.6:p.Ala169=
ENST00000377824.8:n.543C=
ENST00000460882.5:n.533C=
ENST00000480596.5:n.1207C=
ENST00000491488.5:n.211C=
ENST00000494290.1:c.77C=	ENSP00000432021.1:p.Ala26=
ENST00000497693.1:n.2039C=
ENST00000607784.1:c.506C=	ENSP00000475569.1:p.Ala169=
NM_012203.1:c.506C=	NP_036335.1:p.Ala169=
XM_005251631.1:c.185C=	XP_005251688.1:p.Ala62=
XM_011518073.1:c.104C=	XP_011516375.1:p.Ala35=
XR_929374.1:n.951C=
XM_017015320.2:c.506C=	XP_016870809.1:p.Ala169=
XM_017015321.2:c.506C=	XP_016870810.1:p.Ala169=
XM_017015323.2:c.104C=	XP_016870812.1:p.Ala35=
XM_024447716.1:c.779C=	XP_024303484.1:p.Ala260=
XM_024447717.1:c.779C=	XP_024303485.1:p.Ala260=
XR_002956828.1:n.794C=
XR_002956829.1:n.794C=
XR_002956830.1:n.565C=
XR_002956831.1:n.240C=
XR_002956832.1:n.925C=
NM_012203.2:c.506C= MANE Select	NP_036335.1:p.Ala169=