Canonical Allele Identifier: CA1829208349

Gene: GLIS3

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.4291419_4291421delinsCAG , CM000671.2:g.4291419_4291421delinsCAG	GRCh38
NC_000009.11:g.4291419_4291421delinsCAG , CM000671.1:g.4291419_4291421delinsCAG	GRCh37
NC_000009.10:g.4281419_4281421delinsCAG	NCBI36
NG_011782.1:g.13615_13617delinsCTG
NG_011782.2:g.13615_13617delinsCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000491889.6:c.-98-4898_-98-4896delinsCTG	ENSP00000419914.1:n.-98-4898_-98-4896delinsCTG
ENST00000682749.1:c.-78+8000_-78+8002delinsCTG	ENSP00000507306.1:n.-78+8000_-78+8002delinsCTG
ENST00000381971.8:c.-98-4898_-98-4896delinsCTG MANE Select	ENSP00000371398.3:n.-98-4898_-98-4896delinsCTG
ENST00000381971.7:c.-98-4898_-98-4896delinsCTG	ENSP00000371398.3:n.-98-4898_-98-4896delinsCTG
ENST00000465708.5:n.497-4898_497-4896delinsCTG
ENST00000471664.1:n.585-4898_585-4896delinsCTG
ENST00000477901.5:c.-98-4898_-98-4896delinsCTG	ENSP00000417794.1:n.-98-4898_-98-4896delinsCTG
ENST00000478844.5:c.-78+6963_-78+6965delinsCTG	ENSP00000418005.1:n.-78+6963_-78+6965delinsCTG
ENST00000481827.5:c.-98-4898_-98-4896delinsCTG	ENSP00000417883.1:n.-98-4898_-98-4896delinsCTG
ENST00000490709.1:n.416+8000_416+8002delinsCTG
ENST00000491889.5:c.-98-4898_-98-4896delinsCTG	ENSP00000419914.1:n.-98-4898_-98-4896delinsCTG
NM_001042413.1:c.-98-4898_-98-4896delinsCTG	NP_001035878.1:n.-98-4898_-98-4896delinsCTG
XM_005251386.3:c.-78+8000_-78+8002delinsCTG	XP_005251443.1:n.-78+8000_-78+8002delinsCTG
XM_005251387.3:c.-556-4898_-556-4896delinsCTG	XP_005251444.1:n.-556-4898_-556-4896delinsCTG
XM_005251388.3:c.-71+8000_-71+8002delinsCTG	XP_005251445.1:n.-71+8000_-71+8002delinsCTG
XM_005251389.3:c.-98-4898_-98-4896delinsCTG	XP_005251446.1:n.-98-4898_-98-4896delinsCTG
XM_006716731.2:c.-98-4898_-98-4896delinsCTG	XP_006716794.1:n.-98-4898_-98-4896delinsCTG
XM_011517763.1:c.-98-4898_-98-4896delinsCTG	XP_011516065.1:n.-98-4898_-98-4896delinsCTG
XM_011517764.1:c.-98-4898_-98-4896delinsCTG	XP_011516066.1:n.-98-4898_-98-4896delinsCTG
XM_011517765.1:c.-98-4898_-98-4896delinsCTG	XP_011516067.1:n.-98-4898_-98-4896delinsCTG
XM_011517767.1:c.-556-4898_-556-4896delinsCTG	XP_011516069.1:n.-556-4898_-556-4896delinsCTG
XM_011517768.1:c.-98-4898_-98-4896delinsCTG	XP_011516070.1:n.-98-4898_-98-4896delinsCTG
XM_011517769.1:c.-98-4898_-98-4896delinsCTG	XP_011516071.1:n.-98-4898_-98-4896delinsCTG
XR_929206.1:n.669-4898_669-4896delinsCTG
XM_005251386.4:c.-78+8000_-78+8002delinsCTG	XP_005251443.1:n.-78+8000_-78+8002delinsCTG
XM_005251387.4:c.-556-4898_-556-4896delinsCTG	XP_005251444.1:n.-556-4898_-556-4896delinsCTG
XM_005251388.4:c.-71+8000_-71+8002delinsCTG	XP_005251445.1:n.-71+8000_-71+8002delinsCTG
XM_005251389.5:c.-98-4898_-98-4896delinsCTG	XP_005251446.1:n.-98-4898_-98-4896delinsCTG
XM_006716731.3:c.-98-4898_-98-4896delinsCTG	XP_006716794.1:n.-98-4898_-98-4896delinsCTG
XM_011517763.2:c.-98-4898_-98-4896delinsCTG	XP_011516065.1:n.-98-4898_-98-4896delinsCTG
XM_011517764.2:c.-98-4898_-98-4896delinsCTG	XP_011516066.1:n.-98-4898_-98-4896delinsCTG
XM_011517765.2:c.-98-4898_-98-4896delinsCTG	XP_011516067.1:n.-98-4898_-98-4896delinsCTG
XM_011517767.3:c.-556-4898_-556-4896delinsCTG	XP_011516069.1:n.-556-4898_-556-4896delinsCTG
XM_011517769.2:c.-98-4898_-98-4896delinsCTG	XP_011516071.1:n.-98-4898_-98-4896delinsCTG
XR_929206.2:n.665-4898_665-4896delinsCTG
NM_001042413.2:c.-98-4898_-98-4896delinsCTG MANE Select	NP_001035878.1:n.-98-4898_-98-4896delinsCTG