Canonical Allele Identifier: CA463714793

Gene: GLIS3

Linked Data

• MyVariant Identifiers: chr9:g.3856130A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.3856130A>T , CM000671.2:g.3856130A>T	GRCh38
NC_000009.11:g.3856130A>T , CM000671.1:g.3856130A>T	GRCh37
NC_000009.10:g.3846130A>T	NCBI36
NG_011782.1:g.448906T>A
NG_011782.2:g.448906T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000464391.2:n.910T>A
ENST00000491889.6:c.*1715T>A	ENSP00000419914.1:n.*1715T>A
ENST00000645252.2:n.794T>A
ENST00000682749.1:c.1887T>A	ENSP00000507306.1:p.Ala629=
ENST00000682846.1:c.132-26638T>A	ENSP00000507527.1:n.132-26638T>A
ENST00000682864.1:n.851T>A
ENST00000381971.8:c.2352T>A MANE Select	ENSP00000371398.3:p.Ala784=
ENST00000645252.1:n.794T>A
ENST00000324333.14:c.1887T>A	ENSP00000325494.10:p.Ala629=
ENST00000381971.7:c.2352T>A	ENSP00000371398.3:p.Ala784=
ENST00000461870.5:n.708T>A
ENST00000467497.6:n.892T>A
NM_001042413.1:c.2352T>A	NP_001035878.1:p.Ala784=
NM_152629.3:c.1887T>A	NP_689842.3:p.Ala629=
XM_005251386.3:c.1887T>A	XP_005251443.1:p.Ala629=
XM_005251387.3:c.1686T>A	XP_005251444.1:p.Ala562=
XM_005251388.3:c.1686T>A	XP_005251445.1:p.Ala562=
XM_011517763.1:c.2352T>A	XP_011516065.1:p.Ala784=
XM_011517764.1:c.2352T>A	XP_011516066.1:p.Ala784=
XM_011517765.1:c.2352T>A	XP_011516067.1:p.Ala784=
XM_011517766.1:c.1887T>A	XP_011516068.1:p.Ala629=
XM_011517767.1:c.1686T>A	XP_011516069.1:p.Ala562=
XM_005251386.4:c.1887T>A	XP_005251443.1:p.Ala629=
XM_005251387.4:c.1686T>A	XP_005251444.1:p.Ala562=
XM_005251388.4:c.1686T>A	XP_005251445.1:p.Ala562=
XM_011517763.2:c.2352T>A	XP_011516065.1:p.Ala784=
XM_011517764.2:c.2352T>A	XP_011516066.1:p.Ala784=
XM_011517765.2:c.2352T>A	XP_011516067.1:p.Ala784=
XM_011517766.2:c.1887T>A	XP_011516068.1:p.Ala629=
XM_011517767.3:c.1686T>A	XP_011516069.1:p.Ala562=
XM_017014361.1:c.1887T>A	XP_016869850.1:p.Ala629=
NM_001042413.2:c.2352T>A MANE Select	NP_001035878.1:p.Ala784=
NM_152629.4:c.1887T>A	NP_689842.3:p.Ala629=