Canonical Allele Identifier: CA8618403

Gene: KANSL1

Linked Data

• ClinVar Variation Id: 1502444
• ClinVar RCV Id: RCV002045173
• dbSNP Id: rs148203818
• ExAC: 17:44109483 C / T
• gnomAD v2: 17-44109483-C-T
• gnomAD v3: 17-46032117-C-T
• gnomAD v4: 17-46032117-C-T
• MyVariant Identifiers: chr17:g.44109483C>T (hg19) ; chr17:g.46032117C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.46032117C>T , CM000679.2:g.46032117C>T	GRCh38
NC_000017.10:g.44109483C>T , CM000679.1:g.44109483C>T	GRCh37
NC_000017.9:g.41465330C>T	NCBI36
NG_032784.1:g.198258G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000432791.7:c.3020G>A MANE Select	ENSP00000387393.3:p.Arg1007Gln
ENST00000572904.6:c.3020G>A	ENSP00000461484.1:p.Arg1007Gln
ENST00000574590.6:c.3017G>A	ENSP00000461812.2:p.Arg1006Gln
ENST00000575318.6:c.2828G>A	ENSP00000461299.1:p.Arg943Gln
ENST00000638275.1:c.2828G>A	ENSP00000492576.1:p.Arg943Gln
ENST00000639467.1:c.677G>A
ENST00000639805.1:n.437G>A
ENST00000648792.1:c.2888G>A	ENSP00000497628.1:p.Arg963Gln
ENST00000262419.10:c.3020G>A	ENSP00000262419.6:p.Arg1007Gln
ENST00000432791.5:c.3017G>A	ENSP00000387393.2:p.Arg1006Gln
ENST00000572218.5:n.7237G>A
ENST00000572904.5:c.3020G>A	ENSP00000461484.1:p.Arg1007Gln
ENST00000574590.5:c.3020G>A	ENSP00000461812.1:p.Arg1007Gln
ENST00000574963.1:n.450G>A
ENST00000575318.5:c.2828G>A	ENSP00000461299.1:p.Arg943Gln
ENST00000576870.5:n.992G>A
NM_001193465.1:c.3017G>A	NP_001180394.1:p.Arg1006Gln
NM_001193466.1:c.3020G>A	NP_001180395.1:p.Arg1007Gln
NM_015443.3:c.3020G>A	NP_056258.1:p.Arg1007Gln
XM_006721823.1:c.3020G>A	XP_006721886.1:p.Arg1007Gln
XM_006721824.2:c.3020G>A	XP_006721887.1:p.Arg1007Gln
XM_011524628.1:c.3017G>A	XP_011522930.1:p.Arg1006Gln
XM_011524629.1:c.2918G>A	XP_011522931.1:p.Arg973Gln
XM_011524630.1:c.2831G>A	XP_011522932.1:p.Arg944Gln
XM_011524631.1:c.2828G>A	XP_011522933.1:p.Arg943Gln
XM_011524632.1:c.1790G>A	XP_011522934.1:p.Arg597Gln
XM_006721823.2:c.3020G>A	XP_006721886.1:p.Arg1007Gln
XM_006721824.4:c.3020G>A	XP_006721887.1:p.Arg1007Gln
XM_011524628.3:c.3017G>A	XP_011522930.1:p.Arg1006Gln
XM_011524629.3:c.2918G>A	XP_011522931.1:p.Arg973Gln
XM_011524630.3:c.2831G>A	XP_011522932.1:p.Arg944Gln
XM_011524631.3:c.2828G>A	XP_011522933.1:p.Arg943Gln
XM_011524632.3:c.1790G>A	XP_011522934.1:p.Arg597Gln
XM_017024488.2:c.2828G>A	XP_016879977.1:p.Arg943Gln
NM_001193466.2:c.3020G>A	NP_001180395.1:p.Arg1007Gln
NM_015443.4:c.3020G>A MANE Select	NP_056258.1:p.Arg1007Gln
NM_001193465.2:c.3017G>A	NP_001180394.1:p.Arg1006Gln
NM_001379198.1:c.3020G>A	NP_001366127.1:p.Arg1007Gln