Canonical Allele Identifier: CA645596184

Gene: KANSL1

Linked Data

• COSMIC: COSM6034150

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.46032241_46032264dup , CM000679.2:g.46032241_46032264dup	GRCh38
NC_000017.10:g.44109607_44109630dup , CM000679.1:g.44109607_44109630dup	GRCh37
NC_000017.9:g.41465454_41465477dup	NCBI36
NG_032784.1:g.198111_198134dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000432791.7:c.2873_2896dup MANE Select	ENSP00000387393.3:p.Ser965_Thr966insLysLe...
ENST00000572904.6:c.2873_2896dup	ENSP00000461484.1:p.Ser965_Thr966insLysLe...
ENST00000574590.6:c.2870_2893dup	ENSP00000461812.2:p.Ser964_Thr965insLysLe...
ENST00000575318.6:c.2681_2704dup	ENSP00000461299.1:p.Ser901_Thr902insLysLe...
ENST00000638275.1:c.2681_2704dup	ENSP00000492576.1:p.Ser901_Thr902insLysLe...
ENST00000638291.1:n.701_724dup
ENST00000638551.1:n.821_844dup
ENST00000639467.1:c.530_553dup	ENSP00000492741.1:p.Ser184_Thr185insLysLe...
ENST00000639805.1:n.290_313dup
ENST00000648792.1:c.2838-97_2838-74dup	ENSP00000497628.1:n.2838-97_2838-74dup
ENST00000262419.10:c.2873_2896dup	ENSP00000262419.6:p.Ser965_Thr966insLysLe...
ENST00000432791.5:c.2870_2893dup	ENSP00000387393.2:p.Ser964_Thr965insLysLe...
ENST00000572218.5:n.7090_7113dup
ENST00000572904.5:c.2873_2896dup	ENSP00000461484.1:p.Ser965_Thr966insLysLe...
ENST00000573682.1:n.259_282dup
ENST00000574590.5:c.2873_2896dup	ENSP00000461812.1:p.Ser965_Thr966insLysLe...
ENST00000574963.1:n.303_326dup
ENST00000575318.5:c.2681_2704dup	ENSP00000461299.1:p.Ser901_Thr902insLysLe...
ENST00000576870.5:n.845_868dup
NM_001193465.1:c.2870_2893dup	NP_001180394.1:p.Ser964_Thr965insLysLeuGl...
NM_001193466.1:c.2873_2896dup	NP_001180395.1:p.Ser965_Thr966insLysLeuGl...
NM_015443.3:c.2873_2896dup	NP_056258.1:p.Ser965_Thr966insLysLeuGlySe...
XM_006721823.1:c.2873_2896dup	XP_006721886.1:p.Ser965_Thr966insLysLeuGl...
XM_006721824.2:c.2873_2896dup	XP_006721887.1:p.Ser965_Thr966insLysLeuGl...
XM_011524628.1:c.2870_2893dup	XP_011522930.1:p.Ser964_Thr965insLysLeuGl...
XM_011524629.1:c.2771_2794dup	XP_011522931.1:p.Ser931_Thr932insLysLeuGl...
XM_011524630.1:c.2684_2707dup	XP_011522932.1:p.Ser902_Thr903insLysLeuGl...
XM_011524631.1:c.2681_2704dup	XP_011522933.1:p.Ser901_Thr902insLysLeuGl...
XM_011524632.1:c.1643_1666dup	XP_011522934.1:p.Ser555_Thr556insLysLeuGl...
XM_006721823.2:c.2873_2896dup	XP_006721886.1:p.Ser965_Thr966insLysLeuGl...
XM_006721824.4:c.2873_2896dup	XP_006721887.1:p.Ser965_Thr966insLysLeuGl...
XM_011524628.3:c.2870_2893dup	XP_011522930.1:p.Ser964_Thr965insLysLeuGl...
XM_011524629.3:c.2771_2794dup	XP_011522931.1:p.Ser931_Thr932insLysLeuGl...
XM_011524630.3:c.2684_2707dup	XP_011522932.1:p.Ser902_Thr903insLysLeuGl...
XM_011524631.3:c.2681_2704dup	XP_011522933.1:p.Ser901_Thr902insLysLeuGl...
XM_011524632.3:c.1643_1666dup	XP_011522934.1:p.Ser555_Thr556insLysLeuGl...
XM_017024488.2:c.2681_2704dup	XP_016879977.1:p.Ser901_Thr902insLysLeuGl...
NM_001193466.2:c.2873_2896dup	NP_001180395.1:p.Ser965_Thr966insLysLeuGl...
NM_015443.4:c.2873_2896dup MANE Select	NP_056258.1:p.Ser965_Thr966insLysLeuGlySe...
NM_001193465.2:c.2870_2893dup	NP_001180394.1:p.Ser964_Thr965insLysLeuGl...
NM_001379198.1:c.2873_2896dup	NP_001366127.1:p.Ser965_Thr966insLysLeuGl...