Canonical Allele Identifier: CA984119007

Gene: KANSL1

Linked Data

• ClinVar Variation Id: 3022991
• ClinVar RCV Id: RCV003882177
• dbSNP Id: rs2077241144
• gnomAD v3: 17-46039223-G-C
• gnomAD v4: 17-46039223-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.46039223G>C , CM000679.2:g.46039223G>C	GRCh38
NC_000017.10:g.44116589G>C , CM000679.1:g.44116589G>C	GRCh37
NC_000017.9:g.41472436G>C	NCBI36
NG_032784.1:g.191152C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000432791.7:c.2204-8C>G MANE Select	ENSP00000387393.3:n.2204-8C>G
ENST00000572904.6:c.2204-8C>G	ENSP00000461484.1:n.2204-8C>G
ENST00000573286.2:n.3879C>G
ENST00000574590.6:c.2204-8C>G	ENSP00000461812.2:n.2204-8C>G
ENST00000575318.6:c.2203+479C>G	ENSP00000461299.1:n.2203+479C>G
ENST00000638275.1:c.2203+479C>G	ENSP00000492576.1:n.2203+479C>G
ENST00000639150.1:c.938-8C>G	ENSP00000491906.1:n.938-8C>G
ENST00000639531.1:c.2203+479C>G	ENSP00000491765.1:n.2203+479C>G
ENST00000639853.1:c.1374+479C>G
ENST00000640636.1:c.345+479C>G
ENST00000648792.1:c.2204-8C>G	ENSP00000497628.1:n.2204-8C>G
ENST00000262419.10:c.2204-8C>G	ENSP00000262419.6:n.2204-8C>G
ENST00000432791.5:c.2204-8C>G	ENSP00000387393.2:n.2204-8C>G
ENST00000572218.5:n.6421-8C>G
ENST00000572679.1:n.328C>G
ENST00000572904.5:c.2204-8C>G	ENSP00000461484.1:n.2204-8C>G
ENST00000573286.1:n.52C>G
ENST00000574590.5:c.2204-8C>G	ENSP00000461812.1:n.2204-8C>G
ENST00000575318.5:c.2203+479C>G	ENSP00000461299.1:n.2203+479C>G
ENST00000576870.5:n.364+479C>G
NM_001193465.1:c.2204-8C>G	NP_001180394.1:n.2204-8C>G
NM_001193466.1:c.2204-8C>G	NP_001180395.1:n.2204-8C>G
NM_015443.3:c.2204-8C>G	NP_056258.1:n.2204-8C>G
XM_006721823.1:c.2204-8C>G	XP_006721886.1:n.2204-8C>G
XM_006721824.2:c.2204-8C>G	XP_006721887.1:n.2204-8C>G
XM_011524628.1:c.2204-8C>G	XP_011522930.1:n.2204-8C>G
XM_011524629.1:c.2102-8C>G	XP_011522931.1:n.2102-8C>G
XM_011524630.1:c.2203+479C>G	XP_011522932.1:n.2203+479C>G
XM_011524631.1:c.2203+479C>G	XP_011522933.1:n.2203+479C>G
XM_011524632.1:c.974-8C>G	XP_011522934.1:n.974-8C>G
XM_006721823.2:c.2204-8C>G	XP_006721886.1:n.2204-8C>G
XM_006721824.4:c.2204-8C>G	XP_006721887.1:n.2204-8C>G
XM_011524628.3:c.2204-8C>G	XP_011522930.1:n.2204-8C>G
XM_011524629.3:c.2102-8C>G	XP_011522931.1:n.2102-8C>G
XM_011524630.3:c.2203+479C>G	XP_011522932.1:n.2203+479C>G
XM_011524631.3:c.2203+479C>G	XP_011522933.1:n.2203+479C>G
XM_011524632.3:c.974-8C>G	XP_011522934.1:n.974-8C>G
XM_017024488.2:c.2203+479C>G	XP_016879977.1:n.2203+479C>G
XM_017024489.1:c.2102-8C>G	XP_016879978.1:n.2102-8C>G
NM_001193466.2:c.2204-8C>G	NP_001180395.1:n.2204-8C>G
NM_015443.4:c.2204-8C>G MANE Select	NP_056258.1:n.2204-8C>G
NM_001193465.2:c.2204-8C>G	NP_001180394.1:n.2204-8C>G
NM_001379198.1:c.2204-8C>G	NP_001366127.1:n.2204-8C>G