Canonical Allele Identifier: CA2638369741

Gene: KANSL1

Linked Data

• gnomAD v4: 17-46031123-C-CCGCA

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.46031123_46031124insCGCA , CM000679.2:g.46031123_46031124insCGCA	GRCh38
NC_000017.10:g.44108489_44108490insCGCA , CM000679.1:g.44108489_44108490insCGCA	GRCh37
NC_000017.9:g.41464336_41464337insCGCA	NCBI36
NG_032784.1:g.199251_199252insTGCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000432791.7:c.*352_*353insTGCG MANE Select	ENSP00000387393.3:n.*352_*353insTGCG
ENST00000572904.6:c.*352_*353insTGCG	ENSP00000461484.1:n.*352_*353insTGCG
ENST00000574590.6:c.*352_*353insTGCG	ENSP00000461812.2:n.*352_*353insTGCG
ENST00000575318.6:c.*352_*353insTGCG	ENSP00000461299.1:n.*352_*353insTGCG
ENST00000638275.1:c.*352_*353insTGCG	ENSP00000492576.1:n.*352_*353insTGCG
ENST00000648792.1:c.*352_*353insTGCG	ENSP00000497628.1:n.*352_*353insTGCG
ENST00000262419.10:c.*352_*353insTGCG	ENSP00000262419.6:n.*352_*353insTGCG
ENST00000432791.5:c.*352_*353insTGCG	ENSP00000387393.2:n.*352_*353insTGCG
ENST00000572218.5:n.7887_7888insTGCG
ENST00000572904.5:c.*352_*353insTGCG	ENSP00000461484.1:n.*352_*353insTGCG
ENST00000574590.5:c.*352_*353insTGCG	ENSP00000461812.1:n.*352_*353insTGCG
ENST00000574963.1:n.1443_1444insTGCG
ENST00000575318.5:c.*352_*353insTGCG	ENSP00000461299.1:n.*352_*353insTGCG
ENST00000576870.5:n.1642_1643insTGCG
NM_001193465.1:c.*352_*353insTGCG	NP_001180394.1:n.*352_*353insTGCG
NM_001193466.1:c.*352_*353insTGCG	NP_001180395.1:n.*352_*353insTGCG
NM_015443.3:c.*352_*353insTGCG	NP_056258.1:n.*352_*353insTGCG
XM_006721823.1:c.*352_*353insTGCG	XP_006721886.1:n.*352_*353insTGCG
XM_006721824.2:c.*352_*353insTGCG	XP_006721887.1:n.*352_*353insTGCG
XM_011524628.1:c.*352_*353insTGCG	XP_011522930.1:n.*352_*353insTGCG
XM_011524629.1:c.*352_*353insTGCG	XP_011522931.1:n.*352_*353insTGCG
XM_011524630.1:c.*352_*353insTGCG	XP_011522932.1:n.*352_*353insTGCG
XM_011524631.1:c.*352_*353insTGCG	XP_011522933.1:n.*352_*353insTGCG
XM_011524632.1:c.*352_*353insTGCG	XP_011522934.1:n.*352_*353insTGCG
XM_006721823.2:c.*352_*353insTGCG	XP_006721886.1:n.*352_*353insTGCG
XM_006721824.4:c.*352_*353insTGCG	XP_006721887.1:n.*352_*353insTGCG
XM_011524628.3:c.*352_*353insTGCG	XP_011522930.1:n.*352_*353insTGCG
XM_011524629.3:c.*352_*353insTGCG	XP_011522931.1:n.*352_*353insTGCG
XM_011524630.3:c.*352_*353insTGCG	XP_011522932.1:n.*352_*353insTGCG
XM_011524631.3:c.*352_*353insTGCG	XP_011522933.1:n.*352_*353insTGCG
XM_011524632.3:c.*352_*353insTGCG	XP_011522934.1:n.*352_*353insTGCG
XM_017024488.2:c.*352_*353insTGCG	XP_016879977.1:n.*352_*353insTGCG
NM_001193466.2:c.*352_*353insTGCG	NP_001180395.1:n.*352_*353insTGCG
NM_015443.4:c.*352_*353insTGCG MANE Select	NP_056258.1:n.*352_*353insTGCG
NM_001193465.2:c.*352_*353insTGCG	NP_001180394.1:n.*352_*353insTGCG
NM_001379198.1:c.*352_*353insTGCG	NP_001366127.1:n.*352_*353insTGCG