Canonical Allele Identifier: CA4968007

Gene: GLIS3

Linked Data

• dbSNP Id: rs767559985
• ExAC: 9:3932324 GCTT / G
• gnomAD v2: 9-3932324-GCTT-G
• gnomAD v4: 9-3932324-GCTT-G
• MyVariant Identifiers: chr9:g.3932325_3932327del (hg19) ; chr9:g.3932325_3932327del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.3932325_3932327del , CM000671.2:g.3932325_3932327del	GRCh38
NC_000009.11:g.3932325_3932327del , CM000671.1:g.3932325_3932327del	GRCh37
NC_000009.10:g.3922325_3922327del	NCBI36
NG_011782.1:g.372709_372711del
NG_011782.2:g.372709_372711del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000463680.6:n.273+33_273+35del
ENST00000464391.2:n.541+33_541+35del
ENST00000491889.6:c.*1346+33_*1346+35del	ENSP00000419914.1:n.*1346+33_*1346+35del
ENST00000645252.2:n.425+33_425+35del
ENST00000682749.1:c.1518+33_1518+35del	ENSP00000507306.1:n.1518+33_1518+35del
ENST00000682846.1:c.132-102835_132-102833del	ENSP00000507527.1:n.132-102835_132-102833del
ENST00000682864.1:n.482+33_482+35del
ENST00000381971.8:c.1983+33_1983+35del MANE Select	ENSP00000371398.3:n.1983+33_1983+35del
ENST00000645252.1:n.425+33_425+35del
ENST00000324333.14:c.1518+33_1518+35del	ENSP00000325494.10:n.1518+33_1518+35del
ENST00000381971.7:c.1983+33_1983+35del	ENSP00000371398.3:n.1983+33_1983+35del
ENST00000461870.5:n.339+33_339+35del
ENST00000463680.5:n.273+33_273+35del
ENST00000467497.6:n.523+33_523+35del
NM_001042413.1:c.1983+33_1983+35del	NP_001035878.1:n.1983+33_1983+35del
NM_152629.3:c.1518+33_1518+35del	NP_689842.3:n.1518+33_1518+35del
XM_005251386.3:c.1518+33_1518+35del	XP_005251443.1:n.1518+33_1518+35del
XM_005251387.3:c.1317+33_1317+35del	XP_005251444.1:n.1317+33_1317+35del
XM_005251388.3:c.1317+33_1317+35del	XP_005251445.1:n.1317+33_1317+35del
XM_011517763.1:c.1983+33_1983+35del	XP_011516065.1:n.1983+33_1983+35del
XM_011517764.1:c.1983+33_1983+35del	XP_011516066.1:n.1983+33_1983+35del
XM_011517765.1:c.1983+33_1983+35del	XP_011516067.1:n.1983+33_1983+35del
XM_011517766.1:c.1518+33_1518+35del	XP_011516068.1:n.1518+33_1518+35del
XM_011517767.1:c.1317+33_1317+35del	XP_011516069.1:n.1317+33_1317+35del
XM_005251386.4:c.1518+33_1518+35del	XP_005251443.1:n.1518+33_1518+35del
XM_005251387.4:c.1317+33_1317+35del	XP_005251444.1:n.1317+33_1317+35del
XM_005251388.4:c.1317+33_1317+35del	XP_005251445.1:n.1317+33_1317+35del
XM_011517763.2:c.1983+33_1983+35del	XP_011516065.1:n.1983+33_1983+35del
XM_011517764.2:c.1983+33_1983+35del	XP_011516066.1:n.1983+33_1983+35del
XM_011517765.2:c.1983+33_1983+35del	XP_011516067.1:n.1983+33_1983+35del
XM_011517766.2:c.1518+33_1518+35del	XP_011516068.1:n.1518+33_1518+35del
XM_011517767.3:c.1317+33_1317+35del	XP_011516069.1:n.1317+33_1317+35del
XM_017014361.1:c.1518+33_1518+35del	XP_016869850.1:n.1518+33_1518+35del
NM_001042413.2:c.1983+33_1983+35del MANE Select	NP_001035878.1:n.1983+33_1983+35del
NM_152629.4:c.1518+33_1518+35del	NP_689842.3:n.1518+33_1518+35del