Canonical Allele Identifier: CA863886853

Gene: GLIS3

Linked Data

• dbSNP Id: rs1197701583
• MyVariant Identifiers: chr9:g.3932153_3932165del (hg19) ; chr9:g.3932153_3932165del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.3932155_3932167del , CM000671.2:g.3932155_3932167del	GRCh38
NC_000009.11:g.3932155_3932167del , CM000671.1:g.3932155_3932167del	GRCh37
NC_000009.10:g.3922155_3922167del	NCBI36
NG_011782.1:g.372871_372883del
NG_011782.2:g.372871_372883del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000463680.6:n.273+195_273+207del
ENST00000464391.2:n.541+195_541+207del
ENST00000491889.6:c.*1346+195_*1346+207del	ENSP00000419914.1:n.*1346+195_*1346+207del
ENST00000645252.2:n.425+195_425+207del
ENST00000682749.1:c.1518+195_1518+207del	ENSP00000507306.1:n.1518+195_1518+207del
ENST00000682846.1:c.132-102673_132-102661del	ENSP00000507527.1:n.132-102673_132-102661del
ENST00000682864.1:n.482+195_482+207del
ENST00000381971.8:c.1983+195_1983+207del MANE Select	ENSP00000371398.3:n.1983+195_1983+207del
ENST00000645252.1:n.425+195_425+207del
ENST00000324333.14:c.1518+195_1518+207del	ENSP00000325494.10:n.1518+195_1518+207del
ENST00000381971.7:c.1983+195_1983+207del	ENSP00000371398.3:n.1983+195_1983+207del
ENST00000461870.5:n.339+195_339+207del
ENST00000463680.5:n.273+195_273+207del
ENST00000467497.6:n.523+195_523+207del
NM_001042413.1:c.1983+195_1983+207del	NP_001035878.1:n.1983+195_1983+207del
NM_152629.3:c.1518+195_1518+207del	NP_689842.3:n.1518+195_1518+207del
XM_005251386.3:c.1518+195_1518+207del	XP_005251443.1:n.1518+195_1518+207del
XM_005251387.3:c.1317+195_1317+207del	XP_005251444.1:n.1317+195_1317+207del
XM_005251388.3:c.1317+195_1317+207del	XP_005251445.1:n.1317+195_1317+207del
XM_011517763.1:c.1983+195_1983+207del	XP_011516065.1:n.1983+195_1983+207del
XM_011517764.1:c.1983+195_1983+207del	XP_011516066.1:n.1983+195_1983+207del
XM_011517765.1:c.1983+195_1983+207del	XP_011516067.1:n.1983+195_1983+207del
XM_011517766.1:c.1518+195_1518+207del	XP_011516068.1:n.1518+195_1518+207del
XM_011517767.1:c.1317+195_1317+207del	XP_011516069.1:n.1317+195_1317+207del
XM_005251386.4:c.1518+195_1518+207del	XP_005251443.1:n.1518+195_1518+207del
XM_005251387.4:c.1317+195_1317+207del	XP_005251444.1:n.1317+195_1317+207del
XM_005251388.4:c.1317+195_1317+207del	XP_005251445.1:n.1317+195_1317+207del
XM_011517763.2:c.1983+195_1983+207del	XP_011516065.1:n.1983+195_1983+207del
XM_011517764.2:c.1983+195_1983+207del	XP_011516066.1:n.1983+195_1983+207del
XM_011517765.2:c.1983+195_1983+207del	XP_011516067.1:n.1983+195_1983+207del
XM_011517766.2:c.1518+195_1518+207del	XP_011516068.1:n.1518+195_1518+207del
XM_011517767.3:c.1317+195_1317+207del	XP_011516069.1:n.1317+195_1317+207del
XM_017014361.1:c.1518+195_1518+207del	XP_016869850.1:n.1518+195_1518+207del
NM_001042413.2:c.1983+195_1983+207del MANE Select	NP_001035878.1:n.1983+195_1983+207del
NM_152629.4:c.1518+195_1518+207del	NP_689842.3:n.1518+195_1518+207del