Canonical Allele Identifier: CA1846869084

Gene: GRHPR

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37428537A= , CM000671.2:g.37428537A=	GRCh38
NC_000009.11:g.37428534A= , CM000671.1:g.37428534A=	GRCh37
NC_000009.10:g.37418534A=	NCBI36
NG_008135.1:g.10828A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318158.11:c.458A= MANE Select	ENSP00000313432.6:p.Gln153=
ENST00000318158.10:c.458A=	ENSP00000313432.6:p.Gln153=
ENST00000377824.8:n.495A=
ENST00000460882.5:n.485A=
ENST00000491488.5:n.163A=
ENST00000493368.5:n.515A=
ENST00000497693.1:n.832A=
ENST00000607784.1:c.458A=	ENSP00000475569.1:p.Gln153=
NM_012203.1:c.458A=	NP_036335.1:p.Gln153=
XM_005251631.1:c.137A=	XP_005251688.1:p.Gln46=
XM_011518073.1:c.-305A=	XP_011516375.1:n.-305A=
XR_929374.1:n.543A=
XM_017015320.2:c.458A=	XP_016870809.1:p.Gln153=
XM_017015321.2:c.458A=	XP_016870810.1:p.Gln153=
XM_017015323.2:c.-305A=	XP_016870812.1:n.-305A=
XM_024447716.1:c.731A=	XP_024303484.1:p.Gln244=
XM_024447717.1:c.731A=	XP_024303485.1:p.Gln244=
XR_002956828.1:n.746A=
XR_002956829.1:n.746A=
XR_002956830.1:n.517A=
XR_002956831.1:n.192A=
XR_002956832.1:n.517A=
NM_012203.2:c.458A= MANE Select	NP_036335.1:p.Gln153=