Canonical Allele Identifier: CA772450321
Gene: KANSL1 HGNC NCBI

Linked Data

dbSNP Id: rs1235825227

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.46032545_46032546dup , CM000679.2:g.46032545_46032546dup GRCh38
NC_000017.10:g.44109911_44109912dup , CM000679.1:g.44109911_44109912dup GRCh37
NC_000017.9:g.41465758_41465759dup NCBI36
NG_032784.1:g.197829_197830dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000432791.7:c.2838-247_2838-246dup MANE Select ENSP00000387393.3:n.2838-247_2838-246dup
ENST00000572904.6:c.2838-247_2838-246dup ENSP00000461484.1:n.2838-247_2838-246dup
ENST00000574590.6:c.2835-247_2835-246dup ENSP00000461812.2:n.2835-247_2835-246dup
ENST00000575318.6:c.2646-247_2646-246dup ENSP00000461299.1:n.2646-247_2646-246dup
ENST00000638275.1:c.2646-247_2646-246dup ENSP00000492576.1:n.2646-247_2646-246dup
ENST00000638291.1:n.666-247_666-246dup
ENST00000638551.1:n.786-247_786-246dup
ENST00000639467.1:c.495-247_495-246dup ENSP00000492741.1:n.495-247_495-246dup
ENST00000639531.1:c.2649-247_2649-246dup ENSP00000491765.1:n.2649-247_2649-246dup
ENST00000639805.1:n.255-247_255-246dup
ENST00000640092.1:n.1525-247_1525-246dup
ENST00000640751.1:n.433-247_433-246dup
ENST00000648792.1:c.2838-379_2838-378dup ENSP00000497628.1:n.2838-379_2838-378dup
ENST00000262419.10:c.2838-247_2838-246dup ENSP00000262419.6:n.2838-247_2838-246dup
ENST00000432791.5:c.2835-247_2835-246dup ENSP00000387393.2:n.2835-247_2835-246dup
ENST00000572218.5:n.7055-247_7055-246dup
ENST00000572904.5:c.2838-247_2838-246dup ENSP00000461484.1:n.2838-247_2838-246dup
ENST00000573682.1:n.224-247_224-246dup
ENST00000574590.5:c.2838-247_2838-246dup ENSP00000461812.1:n.2838-247_2838-246dup
ENST00000574963.1:n.21_22dup
ENST00000575318.5:c.2646-247_2646-246dup ENSP00000461299.1:n.2646-247_2646-246dup
ENST00000576870.5:n.810-247_810-246dup
NM_001193465.1:c.2835-247_2835-246dup NP_001180394.1:n.2835-247_2835-246dup
NM_001193466.1:c.2838-247_2838-246dup NP_001180395.1:n.2838-247_2838-246dup
NM_015443.3:c.2838-247_2838-246dup NP_056258.1:n.2838-247_2838-246dup
XM_006721823.1:c.2838-247_2838-246dup XP_006721886.1:n.2838-247_2838-246dup
XM_006721824.2:c.2838-247_2838-246dup XP_006721887.1:n.2838-247_2838-246dup
XM_011524628.1:c.2835-247_2835-246dup XP_011522930.1:n.2835-247_2835-246dup
XM_011524629.1:c.2736-247_2736-246dup XP_011522931.1:n.2736-247_2736-246dup
XM_011524630.1:c.2649-247_2649-246dup XP_011522932.1:n.2649-247_2649-246dup
XM_011524631.1:c.2646-247_2646-246dup XP_011522933.1:n.2646-247_2646-246dup
XM_011524632.1:c.1608-247_1608-246dup XP_011522934.1:n.1608-247_1608-246dup
XM_006721823.2:c.2838-247_2838-246dup XP_006721886.1:n.2838-247_2838-246dup
XM_006721824.4:c.2838-247_2838-246dup XP_006721887.1:n.2838-247_2838-246dup
XM_011524628.3:c.2835-247_2835-246dup XP_011522930.1:n.2835-247_2835-246dup
XM_011524629.3:c.2736-247_2736-246dup XP_011522931.1:n.2736-247_2736-246dup
XM_011524630.3:c.2649-247_2649-246dup XP_011522932.1:n.2649-247_2649-246dup
XM_011524631.3:c.2646-247_2646-246dup XP_011522933.1:n.2646-247_2646-246dup
XM_011524632.3:c.1608-247_1608-246dup XP_011522934.1:n.1608-247_1608-246dup
XM_017024488.2:c.2646-247_2646-246dup XP_016879977.1:n.2646-247_2646-246dup
NM_001193466.2:c.2838-247_2838-246dup NP_001180395.1:n.2838-247_2838-246dup
NM_015443.4:c.2838-247_2838-246dup MANE Select NP_056258.1:n.2838-247_2838-246dup
NM_001193465.2:c.2835-247_2835-246dup NP_001180394.1:n.2835-247_2835-246dup
NM_001379198.1:c.2838-247_2838-246dup NP_001366127.1:n.2838-247_2838-246dup