Canonical Allele Identifier: CA2262110501

Gene: KANSL1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.46031056_46031058delinsTAA , CM000679.2:g.46031056_46031058delinsTAA	GRCh38
NC_000017.10:g.44108422_44108424delinsTAA , CM000679.1:g.44108422_44108424delinsTAA	GRCh37
NC_000017.9:g.41464269_41464271delinsTAA	NCBI36
NG_032784.1:g.199317_199319delinsTTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000432791.7:c.*418_*420delinsTTA MANE Select	ENSP00000387393.3:n.*418_*420delinsTTA
ENST00000572904.6:c.*418_*420delinsTTA	ENSP00000461484.1:n.*418_*420delinsTTA
ENST00000574590.6:c.*418_*420delinsTTA	ENSP00000461812.2:n.*418_*420delinsTTA
ENST00000575318.6:c.*418_*420delinsTTA	ENSP00000461299.1:n.*418_*420delinsTTA
ENST00000638275.1:c.*418_*420delinsTTA	ENSP00000492576.1:n.*418_*420delinsTTA
ENST00000648792.1:c.*418_*420delinsTTA	ENSP00000497628.1:n.*418_*420delinsTTA
ENST00000262419.10:c.*418_*420delinsTTA	ENSP00000262419.6:n.*418_*420delinsTTA
ENST00000432791.5:c.*418_*420delinsTTA	ENSP00000387393.2:n.*418_*420delinsTTA
ENST00000572218.5:n.7953_7955delinsTTA
ENST00000572904.5:c.*418_*420delinsTTA	ENSP00000461484.1:n.*418_*420delinsTTA
ENST00000574590.5:c.*418_*420delinsTTA	ENSP00000461812.1:n.*418_*420delinsTTA
ENST00000575318.5:c.*418_*420delinsTTA	ENSP00000461299.1:n.*418_*420delinsTTA
ENST00000576870.5:n.1708_1710delinsTTA
NM_001193465.1:c.*418_*420delinsTTA	NP_001180394.1:n.*418_*420delinsTTA
NM_001193466.1:c.*418_*420delinsTTA	NP_001180395.1:n.*418_*420delinsTTA
NM_015443.3:c.*418_*420delinsTTA	NP_056258.1:n.*418_*420delinsTTA
XM_006721823.1:c.*418_*420delinsTTA	XP_006721886.1:n.*418_*420delinsTTA
XM_006721824.2:c.*418_*420delinsTTA	XP_006721887.1:n.*418_*420delinsTTA
XM_011524628.1:c.*418_*420delinsTTA	XP_011522930.1:n.*418_*420delinsTTA
XM_011524629.1:c.*418_*420delinsTTA	XP_011522931.1:n.*418_*420delinsTTA
XM_011524630.1:c.*418_*420delinsTTA	XP_011522932.1:n.*418_*420delinsTTA
XM_011524631.1:c.*418_*420delinsTTA	XP_011522933.1:n.*418_*420delinsTTA
XM_011524632.1:c.*418_*420delinsTTA	XP_011522934.1:n.*418_*420delinsTTA
XM_006721823.2:c.*418_*420delinsTTA	XP_006721886.1:n.*418_*420delinsTTA
XM_006721824.4:c.*418_*420delinsTTA	XP_006721887.1:n.*418_*420delinsTTA
XM_011524628.3:c.*418_*420delinsTTA	XP_011522930.1:n.*418_*420delinsTTA
XM_011524629.3:c.*418_*420delinsTTA	XP_011522931.1:n.*418_*420delinsTTA
XM_011524630.3:c.*418_*420delinsTTA	XP_011522932.1:n.*418_*420delinsTTA
XM_011524631.3:c.*418_*420delinsTTA	XP_011522933.1:n.*418_*420delinsTTA
XM_011524632.3:c.*418_*420delinsTTA	XP_011522934.1:n.*418_*420delinsTTA
XM_017024488.2:c.*418_*420delinsTTA	XP_016879977.1:n.*418_*420delinsTTA
NM_001193466.2:c.*418_*420delinsTTA	NP_001180395.1:n.*418_*420delinsTTA
NM_015443.4:c.*418_*420delinsTTA MANE Select	NP_056258.1:n.*418_*420delinsTTA
NM_001193465.2:c.*418_*420delinsTTA	NP_001180394.1:n.*418_*420delinsTTA
NM_001379198.1:c.*418_*420delinsTTA	NP_001366127.1:n.*418_*420delinsTTA