Canonical Allele Identifier: CA500369948

Gene: KANSL1

Linked Data

• MyVariant Identifiers: chr17:g.44116514C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.46039148C>G , CM000679.2:g.46039148C>G	GRCh38
NC_000017.10:g.44116514C>G , CM000679.1:g.44116514C>G	GRCh37
NC_000017.9:g.41472361C>G	NCBI36
NG_032784.1:g.191227G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000432791.7:c.2271G>C MANE Select	ENSP00000387393.3:p.Val757=
ENST00000572904.6:c.2271G>C	ENSP00000461484.1:p.Val757=
ENST00000573286.2:n.3954G>C
ENST00000574590.6:c.2271G>C	ENSP00000461812.2:p.Val757=
ENST00000575318.6:c.2204-462G>C	ENSP00000461299.1:n.2204-462G>C
ENST00000638275.1:c.2204-462G>C	ENSP00000492576.1:n.2204-462G>C
ENST00000639150.1:c.1005G>C	ENSP00000491906.1:p.Val335=
ENST00000639531.1:c.2204-462G>C	ENSP00000491765.1:n.2204-462G>C
ENST00000639853.1:c.1375-462G>C
ENST00000640636.1:c.346-462G>C
ENST00000648792.1:c.2271G>C	ENSP00000497628.1:p.Val757=
ENST00000262419.10:c.2271G>C	ENSP00000262419.6:p.Val757=
ENST00000432791.5:c.2271G>C	ENSP00000387393.2:p.Val757=
ENST00000572218.5:n.6488G>C
ENST00000572679.1:n.403G>C
ENST00000572904.5:c.2271G>C	ENSP00000461484.1:p.Val757=
ENST00000573286.1:n.127G>C
ENST00000574590.5:c.2271G>C	ENSP00000461812.1:p.Val757=
ENST00000575318.5:c.2204-462G>C	ENSP00000461299.1:n.2204-462G>C
ENST00000576870.5:n.365-462G>C
NM_001193465.1:c.2271G>C	NP_001180394.1:p.Val757=
NM_001193466.1:c.2271G>C	NP_001180395.1:p.Val757=
NM_015443.3:c.2271G>C	NP_056258.1:p.Val757=
XM_006721823.1:c.2271G>C	XP_006721886.1:p.Val757=
XM_006721824.2:c.2271G>C	XP_006721887.1:p.Val757=
XM_011524628.1:c.2271G>C	XP_011522930.1:p.Val757=
XM_011524629.1:c.2169G>C	XP_011522931.1:p.Val723=
XM_011524630.1:c.2204-462G>C	XP_011522932.1:n.2204-462G>C
XM_011524631.1:c.2204-462G>C	XP_011522933.1:n.2204-462G>C
XM_011524632.1:c.1041G>C	XP_011522934.1:p.Val347=
XM_006721823.2:c.2271G>C	XP_006721886.1:p.Val757=
XM_006721824.4:c.2271G>C	XP_006721887.1:p.Val757=
XM_011524628.3:c.2271G>C	XP_011522930.1:p.Val757=
XM_011524629.3:c.2169G>C	XP_011522931.1:p.Val723=
XM_011524630.3:c.2204-462G>C	XP_011522932.1:n.2204-462G>C
XM_011524631.3:c.2204-462G>C	XP_011522933.1:n.2204-462G>C
XM_011524632.3:c.1041G>C	XP_011522934.1:p.Val347=
XM_017024488.2:c.2204-462G>C	XP_016879977.1:n.2204-462G>C
XM_017024489.1:c.2169G>C	XP_016879978.1:p.Val723=
NM_001193466.2:c.2271G>C	NP_001180395.1:p.Val757=
NM_015443.4:c.2271G>C MANE Select	NP_056258.1:p.Val757=
NM_001193465.2:c.2271G>C	NP_001180394.1:p.Val757=
NM_001379198.1:c.2271G>C	NP_001366127.1:p.Val757=