Canonical Allele Identifier: CA1846874121

Gene: GRHPR

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37432069G= , CM000671.2:g.37432069G=	GRCh38
NC_000009.11:g.37432066G= , CM000671.1:g.37432066G=	GRCh37
NC_000009.10:g.37422066G=	NCBI36
NG_008135.1:g.14360G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318158.11:c.796G= MANE Select	ENSP00000313432.6:p.Ala266=
ENST00000318158.10:c.796G=	ENSP00000313432.6:p.Ala266=
ENST00000460882.5:n.823G=
ENST00000480596.5:n.1497G=
ENST00000482603.1:n.249G=
ENST00000491488.5:n.501G=
ENST00000494290.1:c.*51+918G=	ENSP00000432021.1:n.*51+918G=
ENST00000497693.1:n.4364G=
ENST00000607784.1:c.796G=	ENSP00000475569.1:p.Ala266=
NM_012203.1:c.796G=	NP_036335.1:p.Ala266=
XM_005251631.1:c.475G=	XP_005251688.1:p.Ala159=
XM_011518073.1:c.394G=	XP_011516375.1:p.Ala132=
XM_017015320.2:c.796G=	XP_016870809.1:p.Ala266=
XM_017015321.2:c.796G=	XP_016870810.1:p.Ala266=
XM_017015323.2:c.394G=	XP_016870812.1:p.Ala132=
XM_024447716.1:c.1069G=	XP_024303484.1:p.Ala357=
XM_024447717.1:c.1069G=	XP_024303485.1:p.Ala357=
XR_002956828.1:n.1084G=
XR_002956829.1:n.1084G=
XR_002956830.1:n.2216G=
XR_002956831.1:n.1891G=
XR_002956832.1:n.1215G=
NM_012203.2:c.796G= MANE Select	NP_036335.1:p.Ala266=