Canonical Allele Identifier: CA1846870458

Gene: GRHPR

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37429743G= , CM000671.2:g.37429743G=	GRCh38
NC_000009.11:g.37429740G= , CM000671.1:g.37429740G=	GRCh37
NC_000009.10:g.37419740G=	NCBI36
NG_008135.1:g.12034G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318158.11:c.505G= MANE Select	ENSP00000313432.6:p.Ala169=
ENST00000318158.10:c.505G=	ENSP00000313432.6:p.Ala169=
ENST00000377824.8:n.542G=
ENST00000460882.5:n.532G=
ENST00000480596.5:n.1206G=
ENST00000491488.5:n.210G=
ENST00000494290.1:c.76G=	ENSP00000432021.1:p.Ala26=
ENST00000497693.1:n.2038G=
ENST00000607784.1:c.505G=	ENSP00000475569.1:p.Ala169=
NM_012203.1:c.505G=	NP_036335.1:p.Ala169=
XM_005251631.1:c.184G=	XP_005251688.1:p.Ala62=
XM_011518073.1:c.103G=	XP_011516375.1:p.Ala35=
XR_929374.1:n.950G=
XM_017015320.2:c.505G=	XP_016870809.1:p.Ala169=
XM_017015321.2:c.505G=	XP_016870810.1:p.Ala169=
XM_017015323.2:c.103G=	XP_016870812.1:p.Ala35=
XM_024447716.1:c.778G=	XP_024303484.1:p.Ala260=
XM_024447717.1:c.778G=	XP_024303485.1:p.Ala260=
XR_002956828.1:n.793G=
XR_002956829.1:n.793G=
XR_002956830.1:n.564G=
XR_002956831.1:n.239G=
XR_002956832.1:n.924G=
NM_012203.2:c.505G= MANE Select	NP_036335.1:p.Ala169=