Canonical Allele Identifier: CA399987144

Gene: KANSL1

Linked Data

• MyVariant Identifiers: chr17:g.44109585T>G (hg19) ; chr17:g.46032219T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.46032219T>G , CM000679.2:g.46032219T>G	GRCh38
NC_000017.10:g.44109585T>G , CM000679.1:g.44109585T>G	GRCh37
NC_000017.9:g.41465432T>G	NCBI36
NG_032784.1:g.198156A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000432791.7:c.2918A>C MANE Select	ENSP00000387393.3:p.Asp973Ala
ENST00000572904.6:c.2918A>C	ENSP00000461484.1:p.Asp973Ala
ENST00000574590.6:c.2915A>C	ENSP00000461812.2:p.Asp972Ala
ENST00000575318.6:c.2726A>C	ENSP00000461299.1:p.Asp909Ala
ENST00000638275.1:c.2726A>C	ENSP00000492576.1:p.Asp909Ala
ENST00000638551.1:n.866A>C
ENST00000639467.1:c.575A>C	ENSP00000492741.1:p.Asp192Ala
ENST00000639805.1:n.335A>C
ENST00000648792.1:c.2838-52A>C	ENSP00000497628.1:n.2838-52A>C
ENST00000262419.10:c.2918A>C	ENSP00000262419.6:p.Asp973Ala
ENST00000432791.5:c.2915A>C	ENSP00000387393.2:p.Asp972Ala
ENST00000572218.5:n.7135A>C
ENST00000572904.5:c.2918A>C	ENSP00000461484.1:p.Asp973Ala
ENST00000573682.1:n.304A>C
ENST00000574590.5:c.2918A>C	ENSP00000461812.1:p.Asp973Ala
ENST00000574963.1:n.348A>C
ENST00000575318.5:c.2726A>C	ENSP00000461299.1:p.Asp909Ala
ENST00000576870.5:n.890A>C
NM_001193465.1:c.2915A>C	NP_001180394.1:p.Asp972Ala
NM_001193466.1:c.2918A>C	NP_001180395.1:p.Asp973Ala
NM_015443.3:c.2918A>C	NP_056258.1:p.Asp973Ala
XM_006721823.1:c.2918A>C	XP_006721886.1:p.Asp973Ala
XM_006721824.2:c.2918A>C	XP_006721887.1:p.Asp973Ala
XM_011524628.1:c.2915A>C	XP_011522930.1:p.Asp972Ala
XM_011524629.1:c.2816A>C	XP_011522931.1:p.Asp939Ala
XM_011524630.1:c.2729A>C	XP_011522932.1:p.Asp910Ala
XM_011524631.1:c.2726A>C	XP_011522933.1:p.Asp909Ala
XM_011524632.1:c.1688A>C	XP_011522934.1:p.Asp563Ala
XM_006721823.2:c.2918A>C	XP_006721886.1:p.Asp973Ala
XM_006721824.4:c.2918A>C	XP_006721887.1:p.Asp973Ala
XM_011524628.3:c.2915A>C	XP_011522930.1:p.Asp972Ala
XM_011524629.3:c.2816A>C	XP_011522931.1:p.Asp939Ala
XM_011524630.3:c.2729A>C	XP_011522932.1:p.Asp910Ala
XM_011524631.3:c.2726A>C	XP_011522933.1:p.Asp909Ala
XM_011524632.3:c.1688A>C	XP_011522934.1:p.Asp563Ala
XM_017024488.2:c.2726A>C	XP_016879977.1:p.Asp909Ala
NM_001193466.2:c.2918A>C	NP_001180395.1:p.Asp973Ala
NM_015443.4:c.2918A>C MANE Select	NP_056258.1:p.Asp973Ala
NM_001193465.2:c.2915A>C	NP_001180394.1:p.Asp972Ala
NM_001379198.1:c.2918A>C	NP_001366127.1:p.Asp973Ala