Canonical Allele Identifier: CA1846866339

Gene: GRHPR

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37426545C= , CM000671.2:g.37426545C=	GRCh38
NC_000009.11:g.37426542C= , CM000671.1:g.37426542C=	GRCh37
NC_000009.10:g.37416542C=	NCBI36
NG_008135.1:g.8836C=

Transcript Alleles

HGVS	Amino-acid Change
NM_012203.2:c.295C= MANE Select	NP_036335.1:p.Arg99=
ENST00000318158.11:c.295C= MANE Select	ENSP00000313432.6:p.Arg99=
NM_012203.1:c.295C=	NP_036335.1:p.Arg99=
ENST00000318158.10:c.295C=	ENSP00000313432.6:p.Arg99=
ENST00000377824.8:n.332C=
ENST00000460882.5:n.322C=
ENST00000487399.5:n.847C=
ENST00000491488.5:n.110-1939C=
ENST00000493368.5:n.352C=
ENST00000607784.1:c.295C=	ENSP00000475569.1:p.Arg99=
XM_005251631.1:c.84-1939C=	XP_005251688.1:n.84-1939C=
XM_011518073.1:c.-468C=	XP_011516375.1:n.-468C=
XM_017015320.2:c.295C=	XP_016870809.1:p.Arg99=
XM_017015321.2:c.295C=	XP_016870810.1:p.Arg99=
XM_017015323.2:c.-468C=	XP_016870812.1:n.-468C=
XM_024447716.1:c.568C=	XP_024303484.1:p.Arg190=
XM_024447717.1:c.568C=	XP_024303485.1:p.Arg190=
XR_002956828.1:n.583C=
XR_002956829.1:n.583C=
XR_002956830.1:n.354C=
XR_002956831.1:n.139-1939C=
XR_002956832.1:n.354C=
XR_929374.1:n.380C=