Canonical Allele Identifier: CA2809640640

Gene: KANSL1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.46031726_46031727del , CM000679.2:g.46031726_46031727del	GRCh38
NC_000017.10:g.44109092_44109093del , CM000679.1:g.44109092_44109093del	GRCh37
NC_000017.9:g.41464939_41464940del	NCBI36
NG_032784.1:g.198649_198650del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000432791.7:c.3091-23_3091-22del MANE Select	ENSP00000387393.3:n.3091-23_3091-22del
ENST00000572904.6:c.3091-23_3091-22del	ENSP00000461484.1:n.3091-23_3091-22del
ENST00000574590.6:c.3088-23_3088-22del	ENSP00000461812.2:n.3088-23_3088-22del
ENST00000575318.6:c.2899-23_2899-22del	ENSP00000461299.1:n.2899-23_2899-22del
ENST00000638275.1:c.2899-23_2899-22del	ENSP00000492576.1:n.2899-23_2899-22del
ENST00000639805.1:n.508-23_508-22del
ENST00000648792.1:c.2959-23_2959-22del	ENSP00000497628.1:n.2959-23_2959-22del
ENST00000262419.10:c.3091-23_3091-22del	ENSP00000262419.6:n.3091-23_3091-22del
ENST00000432791.5:c.3088-23_3088-22del	ENSP00000387393.2:n.3088-23_3088-22del
ENST00000572218.5:n.7308-23_7308-22del
ENST00000572904.5:c.3091-23_3091-22del	ENSP00000461484.1:n.3091-23_3091-22del
ENST00000574590.5:c.3091-23_3091-22del	ENSP00000461812.1:n.3091-23_3091-22del
ENST00000574963.1:n.841_842del
ENST00000575318.5:c.2899-23_2899-22del	ENSP00000461299.1:n.2899-23_2899-22del
ENST00000576870.5:n.1063-23_1063-22del
NM_001193465.1:c.3088-23_3088-22del	NP_001180394.1:n.3088-23_3088-22del
NM_001193466.1:c.3091-23_3091-22del	NP_001180395.1:n.3091-23_3091-22del
NM_015443.3:c.3091-23_3091-22del	NP_056258.1:n.3091-23_3091-22del
XM_006721823.1:c.3091-23_3091-22del	XP_006721886.1:n.3091-23_3091-22del
XM_006721824.2:c.3091-23_3091-22del	XP_006721887.1:n.3091-23_3091-22del
XM_011524628.1:c.3088-23_3088-22del	XP_011522930.1:n.3088-23_3088-22del
XM_011524629.1:c.2989-23_2989-22del	XP_011522931.1:n.2989-23_2989-22del
XM_011524630.1:c.2902-23_2902-22del	XP_011522932.1:n.2902-23_2902-22del
XM_011524631.1:c.2899-23_2899-22del	XP_011522933.1:n.2899-23_2899-22del
XM_011524632.1:c.1861-23_1861-22del	XP_011522934.1:n.1861-23_1861-22del
XM_006721823.2:c.3091-23_3091-22del	XP_006721886.1:n.3091-23_3091-22del
XM_006721824.4:c.3091-23_3091-22del	XP_006721887.1:n.3091-23_3091-22del
XM_011524628.3:c.3088-23_3088-22del	XP_011522930.1:n.3088-23_3088-22del
XM_011524629.3:c.2989-23_2989-22del	XP_011522931.1:n.2989-23_2989-22del
XM_011524630.3:c.2902-23_2902-22del	XP_011522932.1:n.2902-23_2902-22del
XM_011524631.3:c.2899-23_2899-22del	XP_011522933.1:n.2899-23_2899-22del
XM_011524632.3:c.1861-23_1861-22del	XP_011522934.1:n.1861-23_1861-22del
XM_017024488.2:c.2899-23_2899-22del	XP_016879977.1:n.2899-23_2899-22del
NM_001193466.2:c.3091-23_3091-22del	NP_001180395.1:n.3091-23_3091-22del
NM_015443.4:c.3091-23_3091-22del MANE Select	NP_056258.1:n.3091-23_3091-22del
NM_001193465.2:c.3088-23_3088-22del	NP_001180394.1:n.3088-23_3088-22del
NM_001379198.1:c.3091-23_3091-22del	NP_001366127.1:n.3091-23_3091-22del