Canonical Allele Identifier: CA1846869446

Gene: GRHPR

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37428798C= , CM000671.2:g.37428798C=	GRCh38
NC_000009.11:g.37428795C= , CM000671.1:g.37428795C=	GRCh37
NC_000009.10:g.37418795C=	NCBI36
NG_008135.1:g.11089C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318158.11:c.493+226C= MANE Select	ENSP00000313432.6:n.493+226C=
ENST00000318158.10:c.493+226C=	ENSP00000313432.6:n.493+226C=
ENST00000377824.8:n.530+226C=
ENST00000460882.5:n.520+226C=
ENST00000480596.5:n.261C=
ENST00000491488.5:n.198+226C=
ENST00000493368.5:n.776C=
ENST00000497693.1:n.1093C=
ENST00000607784.1:c.493+226C=	ENSP00000475569.1:n.493+226C=
NM_012203.1:c.493+226C=	NP_036335.1:n.493+226C=
XM_005251631.1:c.172+226C=	XP_005251688.1:n.172+226C=
XM_011518073.1:c.-44C=	XP_011516375.1:n.-44C=
XR_929374.1:n.804C=
XM_017015320.2:c.493+226C=	XP_016870809.1:n.493+226C=
XM_017015321.2:c.493+226C=	XP_016870810.1:n.493+226C=
XM_017015323.2:c.-44C=	XP_016870812.1:n.-44C=
XM_024447716.1:c.766+226C=	XP_024303484.1:n.766+226C=
XM_024447717.1:c.766+226C=	XP_024303485.1:n.766+226C=
XR_002956828.1:n.781+226C=
XR_002956829.1:n.781+226C=
XR_002956830.1:n.552+226C=
XR_002956831.1:n.227+226C=
XR_002956832.1:n.778C=
NM_012203.2:c.493+226C= MANE Select	NP_036335.1:n.493+226C=