Canonical Allele Identifier: CA1846865852

Gene: GRHPR

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37426009G= , CM000671.2:g.37426009G=	GRCh38
NC_000009.11:g.37426006G= , CM000671.1:g.37426006G=	GRCh37
NC_000009.10:g.37416006G=	NCBI36
NG_008135.1:g.8300G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000318158.11:c.287+15G= MANE Select	ENSP00000313432.6:n.287+15G=
ENST00000318158.10:c.287+15G=	ENSP00000313432.6:n.287+15G=
ENST00000377824.8:n.324+15G=
ENST00000460882.5:n.314+15G=
ENST00000487399.5:n.311G=
ENST00000491488.5:n.110-2475G=
ENST00000493368.5:n.344+15G=
ENST00000607784.1:c.287+15G=	ENSP00000475569.1:n.287+15G=
NM_012203.1:c.287+15G=	NP_036335.1:n.287+15G=
XM_005251631.1:c.84-2475G=	XP_005251688.1:n.84-2475G=
XM_011518073.1:c.-476+15G=	XP_011516375.1:n.-476+15G=
XR_929374.1:n.372+15G=
XM_017015320.2:c.287+15G=	XP_016870809.1:n.287+15G=
XM_017015321.2:c.287+15G=	XP_016870810.1:n.287+15G=
XM_017015323.2:c.-476+15G=	XP_016870812.1:n.-476+15G=
XM_024447716.1:c.560+15G=	XP_024303484.1:n.560+15G=
XM_024447717.1:c.560+15G=	XP_024303485.1:n.560+15G=
XR_002956828.1:n.575+15G=
XR_002956829.1:n.575+15G=
XR_002956830.1:n.346+15G=
XR_002956831.1:n.139-2475G=
XR_002956832.1:n.346+15G=
NM_012203.2:c.287+15G= MANE Select	NP_036335.1:n.287+15G=