Canonical Allele Identifier: CA2262110712

Gene: KANSL1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.46031503_46031506delinsGGCT , CM000679.2:g.46031503_46031506delinsGGCT	GRCh38
NC_000017.10:g.44108869_44108872delinsGGCT , CM000679.1:g.44108869_44108872delinsGGCT	GRCh37
NC_000017.9:g.41464716_41464719delinsGGCT	NCBI36
NG_032784.1:g.198869_198872delinsAGCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000432791.7:c.3288_3291delinsAGCC MANE Select	ENSP00000387393.3:p.Ala1096=
ENST00000572904.6:c.3288_3291delinsAGCC	ENSP00000461484.1:p.Ala1096=
ENST00000574590.6:c.3285_3288delinsAGCC	ENSP00000461812.2:p.Ala1095=
ENST00000575318.6:c.3096_3099delinsAGCC	ENSP00000461299.1:p.Ala1032=
ENST00000638275.1:c.3096_3099delinsAGCC	ENSP00000492576.1:p.Ala1032=
ENST00000648792.1:c.3156_3159delinsAGCC	ENSP00000497628.1:p.Ala1052=
ENST00000262419.10:c.3288_3291delinsAGCC	ENSP00000262419.6:p.Ala1096=
ENST00000432791.5:c.3285_3288delinsAGCC	ENSP00000387393.2:p.Ala1095=
ENST00000572218.5:n.7505_7508delinsAGCC
ENST00000572904.5:c.3288_3291delinsAGCC	ENSP00000461484.1:p.Ala1096=
ENST00000574590.5:c.3288_3291delinsAGCC	ENSP00000461812.1:p.Ala1096=
ENST00000574963.1:n.1061_1064delinsAGCC
ENST00000575318.5:c.3096_3099delinsAGCC	ENSP00000461299.1:p.Ala1032=
ENST00000576870.5:n.1260_1263delinsAGCC
NM_001193465.1:c.3285_3288delinsAGCC	NP_001180394.1:p.Ala1095=
NM_001193466.1:c.3288_3291delinsAGCC	NP_001180395.1:p.Ala1096=
NM_015443.3:c.3288_3291delinsAGCC	NP_056258.1:p.Ala1096=
XM_006721823.1:c.3288_3291delinsAGCC	XP_006721886.1:p.Ala1096=
XM_006721824.2:c.3288_3291delinsAGCC	XP_006721887.1:p.Ala1096=
XM_011524628.1:c.3285_3288delinsAGCC	XP_011522930.1:p.Ala1095=
XM_011524629.1:c.3186_3189delinsAGCC	XP_011522931.1:p.Ala1062=
XM_011524630.1:c.3099_3102delinsAGCC	XP_011522932.1:p.Ala1033=
XM_011524631.1:c.3096_3099delinsAGCC	XP_011522933.1:p.Ala1032=
XM_011524632.1:c.2058_2061delinsAGCC	XP_011522934.1:p.Ala686=
XM_006721823.2:c.3288_3291delinsAGCC	XP_006721886.1:p.Ala1096=
XM_006721824.4:c.3288_3291delinsAGCC	XP_006721887.1:p.Ala1096=
XM_011524628.3:c.3285_3288delinsAGCC	XP_011522930.1:p.Ala1095=
XM_011524629.3:c.3186_3189delinsAGCC	XP_011522931.1:p.Ala1062=
XM_011524630.3:c.3099_3102delinsAGCC	XP_011522932.1:p.Ala1033=
XM_011524631.3:c.3096_3099delinsAGCC	XP_011522933.1:p.Ala1032=
XM_011524632.3:c.2058_2061delinsAGCC	XP_011522934.1:p.Ala686=
XM_017024488.2:c.3096_3099delinsAGCC	XP_016879977.1:p.Ala1032=
NM_001193466.2:c.3288_3291delinsAGCC	NP_001180395.1:p.Ala1096=
NM_015443.4:c.3288_3291delinsAGCC MANE Select	NP_056258.1:p.Ala1096=
NM_001193465.2:c.3285_3288delinsAGCC	NP_001180394.1:p.Ala1095=
NM_001379198.1:c.3288_3291delinsAGCC	NP_001366127.1:p.Ala1096=