Canonical Allele Identifier: CA372808090

Gene: GLIS3

Linked Data

• gnomAD v4: 9-4118780-G-A
• MyVariant Identifiers: chr9:g.4118780G>A (hg19) ; chr9:g.4118780G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.4118780G>A , CM000671.2:g.4118780G>A	GRCh38
NC_000009.11:g.4118780G>A , CM000671.1:g.4118780G>A	GRCh37
NC_000009.10:g.4108780G>A	NCBI36
NG_011782.1:g.186256C>T
NG_011782.2:g.186256C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000491889.6:c.*61C>T	ENSP00000419914.1:n.*61C>T
ENST00000645252.2:n.152+32160C>T
ENST00000682749.1:c.233C>T	ENSP00000507306.1:p.Ala78Val
ENST00000682846.1:c.131+6954C>T	ENSP00000507527.1:n.131+6954C>T
ENST00000381971.8:c.698C>T MANE Select	ENSP00000371398.3:p.Ala233Val
ENST00000645252.1:n.152+32160C>T
ENST00000324333.14:c.233C>T	ENSP00000325494.10:p.Ala78Val
ENST00000381971.7:c.698C>T	ENSP00000371398.3:p.Ala233Val
ENST00000462164.5:c.233C>T	ENSP00000418671.1:p.Ala78Val
ENST00000473846.5:n.457C>T
ENST00000477901.5:c.698C>T	ENSP00000417794.1:p.Ala233Val
ENST00000478315.5:c.233C>T	ENSP00000418995.1:p.Ala78Val
ENST00000478844.5:c.233C>T	ENSP00000418005.1:p.Ala78Val
ENST00000481827.5:c.698C>T	ENSP00000417883.1:p.Ala233Val
ENST00000490709.1:n.518C>T
ENST00000491889.5:c.*61C>T	ENSP00000419914.1:n.*61C>T
NM_001042413.1:c.698C>T	NP_001035878.1:p.Ala233Val
NM_152629.3:c.233C>T	NP_689842.3:p.Ala78Val
XM_005251386.3:c.233C>T	XP_005251443.1:p.Ala78Val
XM_005251387.3:c.32C>T	XP_005251444.1:p.Ala11Val
XM_005251388.3:c.32C>T	XP_005251445.1:p.Ala11Val
XM_005251389.3:c.698C>T	XP_005251446.1:p.Ala233Val
XM_006716731.2:c.698C>T	XP_006716794.1:p.Ala233Val
XM_011517763.1:c.698C>T	XP_011516065.1:p.Ala233Val
XM_011517764.1:c.698C>T	XP_011516066.1:p.Ala233Val
XM_011517765.1:c.698C>T	XP_011516067.1:p.Ala233Val
XM_011517766.1:c.233C>T	XP_011516068.1:p.Ala78Val
XM_011517767.1:c.32C>T	XP_011516069.1:p.Ala11Val
XM_011517768.1:c.698C>T	XP_011516070.1:p.Ala233Val
XM_011517769.1:c.698C>T	XP_011516071.1:p.Ala233Val
XR_929206.1:n.1464C>T
XM_005251386.4:c.233C>T	XP_005251443.1:p.Ala78Val
XM_005251387.4:c.32C>T	XP_005251444.1:p.Ala11Val
XM_005251388.4:c.32C>T	XP_005251445.1:p.Ala11Val
XM_005251389.5:c.698C>T	XP_005251446.1:p.Ala233Val
XM_006716731.3:c.698C>T	XP_006716794.1:p.Ala233Val
XM_011517763.2:c.698C>T	XP_011516065.1:p.Ala233Val
XM_011517764.2:c.698C>T	XP_011516066.1:p.Ala233Val
XM_011517765.2:c.698C>T	XP_011516067.1:p.Ala233Val
XM_011517766.2:c.233C>T	XP_011516068.1:p.Ala78Val
XM_011517767.3:c.32C>T	XP_011516069.1:p.Ala11Val
XM_011517769.2:c.698C>T	XP_011516071.1:p.Ala233Val
XM_017014361.1:c.233C>T	XP_016869850.1:p.Ala78Val
XR_929206.2:n.1460C>T
NM_001042413.2:c.698C>T MANE Select	NP_001035878.1:p.Ala233Val
NM_152629.4:c.233C>T	NP_689842.3:p.Ala78Val