Canonical Allele Identifier: CA1829088752

Gene: GLIS3

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.4117847C= , CM000671.2:g.4117847C=	GRCh38
NC_000009.11:g.4117847C= , CM000671.1:g.4117847C=	GRCh37
NC_000009.10:g.4107847C=	NCBI36
NG_011782.1:g.187189G=
NG_011782.2:g.187189G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000491889.6:c.*994G=	ENSP00000419914.1:n.*994G=
ENST00000645252.2:n.152+33093G=
ENST00000682749.1:c.1166G=	ENSP00000507306.1:p.Arg389=
ENST00000682846.1:c.131+7887G=	ENSP00000507527.1:n.131+7887G=
ENST00000381971.8:c.1631G= MANE Select	ENSP00000371398.3:p.Arg544=
ENST00000645252.1:n.152+33093G=
ENST00000324333.14:c.1166G=	ENSP00000325494.10:p.Arg389=
ENST00000381971.7:c.1631G=	ENSP00000371398.3:p.Arg544=
ENST00000467497.6:n.171G=
NM_001042413.1:c.1631G=	NP_001035878.1:p.Arg544=
NM_152629.3:c.1166G=	NP_689842.3:p.Arg389=
XM_005251386.3:c.1166G=	XP_005251443.1:p.Arg389=
XM_005251387.3:c.965G=	XP_005251444.1:p.Arg322=
XM_005251388.3:c.965G=	XP_005251445.1:p.Arg322=
XM_005251389.3:c.1631G=	XP_005251446.1:p.Arg544=
XM_006716731.2:c.1631G=	XP_006716794.1:p.Arg544=
XM_011517763.1:c.1631G=	XP_011516065.1:p.Arg544=
XM_011517764.1:c.1631G=	XP_011516066.1:p.Arg544=
XM_011517765.1:c.1631G=	XP_011516067.1:p.Arg544=
XM_011517766.1:c.1166G=	XP_011516068.1:p.Arg389=
XM_011517767.1:c.965G=	XP_011516069.1:p.Arg322=
XM_011517768.1:c.1631G=	XP_011516070.1:p.Arg544=
XM_011517769.1:c.1631G=	XP_011516071.1:p.Arg544=
XR_929206.1:n.2397G=
XM_005251386.4:c.1166G=	XP_005251443.1:p.Arg389=
XM_005251387.4:c.965G=	XP_005251444.1:p.Arg322=
XM_005251388.4:c.965G=	XP_005251445.1:p.Arg322=
XM_005251389.5:c.1631G=	XP_005251446.1:p.Arg544=
XM_006716731.3:c.1631G=	XP_006716794.1:p.Arg544=
XM_011517763.2:c.1631G=	XP_011516065.1:p.Arg544=
XM_011517764.2:c.1631G=	XP_011516066.1:p.Arg544=
XM_011517765.2:c.1631G=	XP_011516067.1:p.Arg544=
XM_011517766.2:c.1166G=	XP_011516068.1:p.Arg389=
XM_011517767.3:c.965G=	XP_011516069.1:p.Arg322=
XM_011517769.2:c.1631G=	XP_011516071.1:p.Arg544=
XM_017014361.1:c.1166G=	XP_016869850.1:p.Arg389=
XR_929206.2:n.2393G=
NM_001042413.2:c.1631G= MANE Select	NP_001035878.1:p.Arg544=
NM_152629.4:c.1166G=	NP_689842.3:p.Arg389=