Canonical Allele Identifier: CA772450230

Gene: KANSL1

Linked Data

• dbSNP Id: rs993250448
• MyVariant Identifiers: chr17:g.44109688C>T (hg19) ; chr17:g.46032322C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.46032322C>T , CM000679.2:g.46032322C>T	GRCh38
NC_000017.10:g.44109688C>T , CM000679.1:g.44109688C>T	GRCh37
NC_000017.9:g.41465535C>T	NCBI36
NG_032784.1:g.198053G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000432791.7:c.2838-23G>A MANE Select	ENSP00000387393.3:n.2838-23G>A
ENST00000572904.6:c.2838-23G>A	ENSP00000461484.1:n.2838-23G>A
ENST00000574590.6:c.2835-23G>A	ENSP00000461812.2:n.2835-23G>A
ENST00000575318.6:c.2646-23G>A	ENSP00000461299.1:n.2646-23G>A
ENST00000638275.1:c.2646-23G>A	ENSP00000492576.1:n.2646-23G>A
ENST00000638291.1:n.666-23G>A
ENST00000638551.1:n.786-23G>A
ENST00000639467.1:c.495-23G>A	ENSP00000492741.1:n.495-23G>A
ENST00000639531.1:c.2649-23G>A	ENSP00000491765.1:n.2649-23G>A
ENST00000639805.1:n.255-23G>A
ENST00000640092.1:n.1525-23G>A
ENST00000640751.1:n.433-23G>A
ENST00000648792.1:c.2838-155G>A	ENSP00000497628.1:n.2838-155G>A
ENST00000262419.10:c.2838-23G>A	ENSP00000262419.6:n.2838-23G>A
ENST00000432791.5:c.2835-23G>A	ENSP00000387393.2:n.2835-23G>A
ENST00000572218.5:n.7055-23G>A
ENST00000572904.5:c.2838-23G>A	ENSP00000461484.1:n.2838-23G>A
ENST00000573682.1:n.224-23G>A
ENST00000574590.5:c.2838-23G>A	ENSP00000461812.1:n.2838-23G>A
ENST00000574963.1:n.245G>A
ENST00000575318.5:c.2646-23G>A	ENSP00000461299.1:n.2646-23G>A
ENST00000576870.5:n.810-23G>A
NM_001193465.1:c.2835-23G>A	NP_001180394.1:n.2835-23G>A
NM_001193466.1:c.2838-23G>A	NP_001180395.1:n.2838-23G>A
NM_015443.3:c.2838-23G>A	NP_056258.1:n.2838-23G>A
XM_006721823.1:c.2838-23G>A	XP_006721886.1:n.2838-23G>A
XM_006721824.2:c.2838-23G>A	XP_006721887.1:n.2838-23G>A
XM_011524628.1:c.2835-23G>A	XP_011522930.1:n.2835-23G>A
XM_011524629.1:c.2736-23G>A	XP_011522931.1:n.2736-23G>A
XM_011524630.1:c.2649-23G>A	XP_011522932.1:n.2649-23G>A
XM_011524631.1:c.2646-23G>A	XP_011522933.1:n.2646-23G>A
XM_011524632.1:c.1608-23G>A	XP_011522934.1:n.1608-23G>A
XM_006721823.2:c.2838-23G>A	XP_006721886.1:n.2838-23G>A
XM_006721824.4:c.2838-23G>A	XP_006721887.1:n.2838-23G>A
XM_011524628.3:c.2835-23G>A	XP_011522930.1:n.2835-23G>A
XM_011524629.3:c.2736-23G>A	XP_011522931.1:n.2736-23G>A
XM_011524630.3:c.2649-23G>A	XP_011522932.1:n.2649-23G>A
XM_011524631.3:c.2646-23G>A	XP_011522933.1:n.2646-23G>A
XM_011524632.3:c.1608-23G>A	XP_011522934.1:n.1608-23G>A
XM_017024488.2:c.2646-23G>A	XP_016879977.1:n.2646-23G>A
NM_001193466.2:c.2838-23G>A	NP_001180395.1:n.2838-23G>A
NM_015443.4:c.2838-23G>A MANE Select	NP_056258.1:n.2838-23G>A
NM_001193465.2:c.2835-23G>A	NP_001180394.1:n.2835-23G>A
NM_001379198.1:c.2838-23G>A	NP_001366127.1:n.2838-23G>A