Canonical Allele Identifier: CA2638379966

Gene: KANSL1

Linked Data

• gnomAD v4: 17-46038458-C-CTCA

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.46038459_46038461dup , CM000679.2:g.46038459_46038461dup	GRCh38
NC_000017.10:g.44115825_44115827dup , CM000679.1:g.44115825_44115827dup	GRCh37
NC_000017.9:g.41471672_41471674dup	NCBI36
NG_032784.1:g.191914_191916dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000432791.7:c.2541+77_2541+79dup MANE Select	ENSP00000387393.3:n.2541+77_2541+79dup
ENST00000572904.6:c.2541+77_2541+79dup	ENSP00000461484.1:n.2541+77_2541+79dup
ENST00000573286.2:n.4301_4303dup
ENST00000574590.6:c.2541+77_2541+79dup	ENSP00000461812.2:n.2541+77_2541+79dup
ENST00000575318.6:c.2352+77_2352+79dup	ENSP00000461299.1:n.2352+77_2352+79dup
ENST00000576137.2:n.538+77_538+79dup
ENST00000638275.1:c.2352+77_2352+79dup	ENSP00000492576.1:n.2352+77_2352+79dup
ENST00000639150.1:c.1275+77_1275+79dup	ENSP00000491906.1:n.1275+77_1275+79dup
ENST00000639467.1:c.204+77_204+79dup	ENSP00000492741.1:n.204+77_204+79dup
ENST00000639531.1:c.2352+77_2352+79dup	ENSP00000491765.1:n.2352+77_2352+79dup
ENST00000640636.1:c.494+77_494+79dup
ENST00000648792.1:c.2541+77_2541+79dup	ENSP00000497628.1:n.2541+77_2541+79dup
ENST00000262419.10:c.2541+77_2541+79dup	ENSP00000262419.6:n.2541+77_2541+79dup
ENST00000432791.5:c.2541+77_2541+79dup	ENSP00000387393.2:n.2541+77_2541+79dup
ENST00000572218.5:n.6758+77_6758+79dup
ENST00000572904.5:c.2541+77_2541+79dup	ENSP00000461484.1:n.2541+77_2541+79dup
ENST00000573286.1:n.474_476dup
ENST00000574590.5:c.2541+77_2541+79dup	ENSP00000461812.1:n.2541+77_2541+79dup
ENST00000575318.5:c.2352+77_2352+79dup	ENSP00000461299.1:n.2352+77_2352+79dup
ENST00000576137.1:n.180+77_180+79dup
ENST00000576870.5:n.513+77_513+79dup
NM_001193465.1:c.2541+77_2541+79dup	NP_001180394.1:n.2541+77_2541+79dup
NM_001193466.1:c.2541+77_2541+79dup	NP_001180395.1:n.2541+77_2541+79dup
NM_015443.3:c.2541+77_2541+79dup	NP_056258.1:n.2541+77_2541+79dup
XM_006721823.1:c.2541+77_2541+79dup	XP_006721886.1:n.2541+77_2541+79dup
XM_006721824.2:c.2541+77_2541+79dup	XP_006721887.1:n.2541+77_2541+79dup
XM_011524628.1:c.2541+77_2541+79dup	XP_011522930.1:n.2541+77_2541+79dup
XM_011524629.1:c.2439+77_2439+79dup	XP_011522931.1:n.2439+77_2439+79dup
XM_011524630.1:c.2352+77_2352+79dup	XP_011522932.1:n.2352+77_2352+79dup
XM_011524631.1:c.2352+77_2352+79dup	XP_011522933.1:n.2352+77_2352+79dup
XM_011524632.1:c.1311+77_1311+79dup	XP_011522934.1:n.1311+77_1311+79dup
XM_006721823.2:c.2541+77_2541+79dup	XP_006721886.1:n.2541+77_2541+79dup
XM_006721824.4:c.2541+77_2541+79dup	XP_006721887.1:n.2541+77_2541+79dup
XM_011524628.3:c.2541+77_2541+79dup	XP_011522930.1:n.2541+77_2541+79dup
XM_011524629.3:c.2439+77_2439+79dup	XP_011522931.1:n.2439+77_2439+79dup
XM_011524630.3:c.2352+77_2352+79dup	XP_011522932.1:n.2352+77_2352+79dup
XM_011524631.3:c.2352+77_2352+79dup	XP_011522933.1:n.2352+77_2352+79dup
XM_011524632.3:c.1311+77_1311+79dup	XP_011522934.1:n.1311+77_1311+79dup
XM_017024488.2:c.2352+77_2352+79dup	XP_016879977.1:n.2352+77_2352+79dup
XM_017024489.1:c.2516_2518dup	XP_016879978.1:p.Val839_Arg840insMet
NM_001193466.2:c.2541+77_2541+79dup	NP_001180395.1:n.2541+77_2541+79dup
NM_015443.4:c.2541+77_2541+79dup MANE Select	NP_056258.1:n.2541+77_2541+79dup
NM_001193465.2:c.2541+77_2541+79dup	NP_001180394.1:n.2541+77_2541+79dup
NM_001379198.1:c.2541+77_2541+79dup	NP_001366127.1:n.2541+77_2541+79dup