Canonical Allele Identifier: CA1846865075

Gene: GRHPR

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37424991G= , CM000671.2:g.37424991G=	GRCh38
NC_000009.11:g.37424988G= , CM000671.1:g.37424988G=	GRCh37
NC_000009.10:g.37414988G=	NCBI36
NG_008135.1:g.7282G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000318158.11:c.214+16G= MANE Select	ENSP00000313432.6:n.214+16G=
ENST00000318158.10:c.214+16G=	ENSP00000313432.6:n.214+16G=
ENST00000377824.8:n.251+16G=
ENST00000460882.5:n.241+16G=
ENST00000487399.5:n.223+16G=
ENST00000491488.5:n.109+2158G=
ENST00000493368.5:n.271+16G=
ENST00000607784.1:c.214+16G=	ENSP00000475569.1:n.214+16G=
NM_012203.1:c.214+16G=	NP_036335.1:n.214+16G=
XM_005251631.1:c.83+2158G=	XP_005251688.1:n.83+2158G=
XM_011518073.1:c.-549+16G=	XP_011516375.1:n.-549+16G=
XR_929374.1:n.299+16G=
XM_017015320.2:c.214+16G=	XP_016870809.1:n.214+16G=
XM_017015321.2:c.214+16G=	XP_016870810.1:n.214+16G=
XM_017015323.2:c.-549+16G=	XP_016870812.1:n.-549+16G=
XM_024447716.1:c.487+16G=	XP_024303484.1:n.487+16G=
XM_024447717.1:c.487+16G=	XP_024303485.1:n.487+16G=
XR_002956828.1:n.502+16G=
XR_002956829.1:n.502+16G=
XR_002956830.1:n.273+16G=
XR_002956831.1:n.138+2158G=
XR_002956832.1:n.273+16G=
NM_012203.2:c.214+16G= MANE Select	NP_036335.1:n.214+16G=