Canonical Allele Identifier: CA1846865061

Gene: GRHPR

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37424984T= , CM000671.2:g.37424984T=	GRCh38
NC_000009.11:g.37424981T= , CM000671.1:g.37424981T=	GRCh37
NC_000009.10:g.37414981T=	NCBI36
NG_008135.1:g.7275T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000318158.11:c.214+9T= MANE Select	ENSP00000313432.6:n.214+9T=
ENST00000318158.10:c.214+9T=	ENSP00000313432.6:n.214+9T=
ENST00000377824.8:n.251+9T=
ENST00000460882.5:n.241+9T=
ENST00000487399.5:n.223+9T=
ENST00000491488.5:n.109+2151T=
ENST00000493368.5:n.271+9T=
ENST00000607784.1:c.214+9T=	ENSP00000475569.1:n.214+9T=
NM_012203.1:c.214+9T=	NP_036335.1:n.214+9T=
XM_005251631.1:c.83+2151T=	XP_005251688.1:n.83+2151T=
XM_011518073.1:c.-549+9T=	XP_011516375.1:n.-549+9T=
XR_929374.1:n.299+9T=
XM_017015320.2:c.214+9T=	XP_016870809.1:n.214+9T=
XM_017015321.2:c.214+9T=	XP_016870810.1:n.214+9T=
XM_017015323.2:c.-549+9T=	XP_016870812.1:n.-549+9T=
XM_024447716.1:c.487+9T=	XP_024303484.1:n.487+9T=
XM_024447717.1:c.487+9T=	XP_024303485.1:n.487+9T=
XR_002956828.1:n.502+9T=
XR_002956829.1:n.502+9T=
XR_002956830.1:n.273+9T=
XR_002956831.1:n.138+2151T=
XR_002956832.1:n.273+9T=
NM_012203.2:c.214+9T= MANE Select	NP_036335.1:n.214+9T=