Canonical Allele Identifier: CA1846869449

Gene: GRHPR

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37428799T= , CM000671.2:g.37428799T=	GRCh38
NC_000009.11:g.37428796T= , CM000671.1:g.37428796T=	GRCh37
NC_000009.10:g.37418796T=	NCBI36
NG_008135.1:g.11090T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318158.11:c.493+227T= MANE Select	ENSP00000313432.6:n.493+227T=
ENST00000318158.10:c.493+227T=	ENSP00000313432.6:n.493+227T=
ENST00000377824.8:n.530+227T=
ENST00000460882.5:n.520+227T=
ENST00000480596.5:n.262T=
ENST00000491488.5:n.198+227T=
ENST00000493368.5:n.777T=
ENST00000497693.1:n.1094T=
ENST00000607784.1:c.493+227T=	ENSP00000475569.1:n.493+227T=
NM_012203.1:c.493+227T=	NP_036335.1:n.493+227T=
XM_005251631.1:c.172+227T=	XP_005251688.1:n.172+227T=
XM_011518073.1:c.-43T=	XP_011516375.1:n.-43T=
XR_929374.1:n.805T=
XM_017015320.2:c.493+227T=	XP_016870809.1:n.493+227T=
XM_017015321.2:c.493+227T=	XP_016870810.1:n.493+227T=
XM_017015323.2:c.-43T=	XP_016870812.1:n.-43T=
XM_024447716.1:c.766+227T=	XP_024303484.1:n.766+227T=
XM_024447717.1:c.766+227T=	XP_024303485.1:n.766+227T=
XR_002956828.1:n.781+227T=
XR_002956829.1:n.781+227T=
XR_002956830.1:n.552+227T=
XR_002956831.1:n.227+227T=
XR_002956832.1:n.779T=
NM_012203.2:c.493+227T= MANE Select	NP_036335.1:n.493+227T=