Canonical Allele Identifier: CA2638370465

Gene: KANSL1

Linked Data

• gnomAD v4: 17-46031391-A-ACAGT

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.46031391_46031392insCAGT , CM000679.2:g.46031391_46031392insCAGT	GRCh38
NC_000017.10:g.44108757_44108758insCAGT , CM000679.1:g.44108757_44108758insCAGT	GRCh37
NC_000017.9:g.41464604_41464605insCAGT	NCBI36
NG_032784.1:g.198983_198984insACTG

Transcript Alleles

HGVS	Amino-acid change
ENST00000432791.7:c.*84_*85insACTG MANE Select	ENSP00000387393.3:n.*84_*85insACTG
ENST00000572904.6:c.*84_*85insACTG	ENSP00000461484.1:n.*84_*85insACTG
ENST00000574590.6:c.*84_*85insACTG	ENSP00000461812.2:n.*84_*85insACTG
ENST00000575318.6:c.*84_*85insACTG	ENSP00000461299.1:n.*84_*85insACTG
ENST00000638275.1:c.*84_*85insACTG	ENSP00000492576.1:n.*84_*85insACTG
ENST00000648792.1:c.*84_*85insACTG	ENSP00000497628.1:n.*84_*85insACTG
ENST00000262419.10:c.*84_*85insACTG	ENSP00000262419.6:n.*84_*85insACTG
ENST00000432791.5:c.*84_*85insACTG	ENSP00000387393.2:n.*84_*85insACTG
ENST00000572218.5:n.7619_7620insACTG
ENST00000572904.5:c.*84_*85insACTG	ENSP00000461484.1:n.*84_*85insACTG
ENST00000574590.5:c.*84_*85insACTG	ENSP00000461812.1:n.*84_*85insACTG
ENST00000574963.1:n.1175_1176insACTG
ENST00000575318.5:c.*84_*85insACTG	ENSP00000461299.1:n.*84_*85insACTG
ENST00000576870.5:n.1374_1375insACTG
NM_001193465.1:c.*84_*85insACTG	NP_001180394.1:n.*84_*85insACTG
NM_001193466.1:c.*84_*85insACTG	NP_001180395.1:n.*84_*85insACTG
NM_015443.3:c.*84_*85insACTG	NP_056258.1:n.*84_*85insACTG
XM_006721823.1:c.*84_*85insACTG	XP_006721886.1:n.*84_*85insACTG
XM_006721824.2:c.*84_*85insACTG	XP_006721887.1:n.*84_*85insACTG
XM_011524628.1:c.*84_*85insACTG	XP_011522930.1:n.*84_*85insACTG
XM_011524629.1:c.*84_*85insACTG	XP_011522931.1:n.*84_*85insACTG
XM_011524630.1:c.*84_*85insACTG	XP_011522932.1:n.*84_*85insACTG
XM_011524631.1:c.*84_*85insACTG	XP_011522933.1:n.*84_*85insACTG
XM_011524632.1:c.*84_*85insACTG	XP_011522934.1:n.*84_*85insACTG
XM_006721823.2:c.*84_*85insACTG	XP_006721886.1:n.*84_*85insACTG
XM_006721824.4:c.*84_*85insACTG	XP_006721887.1:n.*84_*85insACTG
XM_011524628.3:c.*84_*85insACTG	XP_011522930.1:n.*84_*85insACTG
XM_011524629.3:c.*84_*85insACTG	XP_011522931.1:n.*84_*85insACTG
XM_011524630.3:c.*84_*85insACTG	XP_011522932.1:n.*84_*85insACTG
XM_011524631.3:c.*84_*85insACTG	XP_011522933.1:n.*84_*85insACTG
XM_011524632.3:c.*84_*85insACTG	XP_011522934.1:n.*84_*85insACTG
XM_017024488.2:c.*84_*85insACTG	XP_016879977.1:n.*84_*85insACTG
NM_001193466.2:c.*84_*85insACTG	NP_001180395.1:n.*84_*85insACTG
NM_015443.4:c.*84_*85insACTG MANE Select	NP_056258.1:n.*84_*85insACTG
NM_001193465.2:c.*84_*85insACTG	NP_001180394.1:n.*84_*85insACTG
NM_001379198.1:c.*84_*85insACTG	NP_001366127.1:n.*84_*85insACTG