Canonical Allele Identifier: CA1846869422

Gene: GRHPR

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37428763C= , CM000671.2:g.37428763C=	GRCh38
NC_000009.11:g.37428760C= , CM000671.1:g.37428760C=	GRCh37
NC_000009.10:g.37418760C=	NCBI36
NG_008135.1:g.11054C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318158.11:c.493+191C= MANE Select	ENSP00000313432.6:n.493+191C=
ENST00000318158.10:c.493+191C=	ENSP00000313432.6:n.493+191C=
ENST00000377824.8:n.530+191C=
ENST00000460882.5:n.520+191C=
ENST00000480596.5:n.226C=
ENST00000491488.5:n.198+191C=
ENST00000493368.5:n.741C=
ENST00000497693.1:n.1058C=
ENST00000607784.1:c.493+191C=	ENSP00000475569.1:n.493+191C=
NM_012203.1:c.493+191C=	NP_036335.1:n.493+191C=
XM_005251631.1:c.172+191C=	XP_005251688.1:n.172+191C=
XM_011518073.1:c.-79C=	XP_011516375.1:n.-79C=
XR_929374.1:n.769C=
XM_017015320.2:c.493+191C=	XP_016870809.1:n.493+191C=
XM_017015321.2:c.493+191C=	XP_016870810.1:n.493+191C=
XM_017015323.2:c.-79C=	XP_016870812.1:n.-79C=
XM_024447716.1:c.766+191C=	XP_024303484.1:n.766+191C=
XM_024447717.1:c.766+191C=	XP_024303485.1:n.766+191C=
XR_002956828.1:n.781+191C=
XR_002956829.1:n.781+191C=
XR_002956830.1:n.552+191C=
XR_002956831.1:n.227+191C=
XR_002956832.1:n.743C=
NM_012203.2:c.493+191C= MANE Select	NP_036335.1:n.493+191C=