Canonical Allele Identifier: CA399980670

Gene: KANSL1

Linked Data

• MyVariant Identifiers: chr17:g.44116051C>G (hg19) ; chr17:g.46038685C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.46038685C>G , CM000679.2:g.46038685C>G	GRCh38
NC_000017.10:g.44116051C>G , CM000679.1:g.44116051C>G	GRCh37
NC_000017.9:g.41471898C>G	NCBI36
NG_032784.1:g.191690G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000432791.7:c.2394G>C MANE Select	ENSP00000387393.3:p.Val798=
ENST00000572904.6:c.2394G>C	ENSP00000461484.1:p.Val798=
ENST00000573286.2:n.4077G>C
ENST00000574590.6:c.2394G>C	ENSP00000461812.2:p.Val798=
ENST00000575318.6:c.2205G>C	ENSP00000461299.1:p.Met735Ile
ENST00000576137.2:n.391G>C
ENST00000638275.1:c.2205G>C	ENSP00000492576.1:p.Met735Ile
ENST00000639150.1:c.1128G>C	ENSP00000491906.1:p.Val376=
ENST00000639467.1:c.57G>C	ENSP00000492741.1:p.Val19=
ENST00000639531.1:c.2205G>C	ENSP00000491765.1:p.Met735Ile
ENST00000639853.1:c.1376G>C
ENST00000640636.1:c.347G>C
ENST00000648792.1:c.2394G>C	ENSP00000497628.1:p.Val798=
ENST00000262419.10:c.2394G>C	ENSP00000262419.6:p.Val798=
ENST00000432791.5:c.2394G>C	ENSP00000387393.2:p.Val798=
ENST00000572218.5:n.6611G>C
ENST00000572679.1:n.526G>C
ENST00000572904.5:c.2394G>C	ENSP00000461484.1:p.Val798=
ENST00000573286.1:n.250G>C
ENST00000574590.5:c.2394G>C	ENSP00000461812.1:p.Val798=
ENST00000575318.5:c.2205G>C	ENSP00000461299.1:p.Met735Ile
ENST00000576137.1:n.33G>C
ENST00000576870.5:n.366G>C
NM_001193465.1:c.2394G>C	NP_001180394.1:p.Val798=
NM_001193466.1:c.2394G>C	NP_001180395.1:p.Val798=
NM_015443.3:c.2394G>C	NP_056258.1:p.Val798=
XM_006721823.1:c.2394G>C	XP_006721886.1:p.Val798=
XM_006721824.2:c.2394G>C	XP_006721887.1:p.Val798=
XM_011524628.1:c.2394G>C	XP_011522930.1:p.Val798=
XM_011524629.1:c.2292G>C	XP_011522931.1:p.Val764=
XM_011524630.1:c.2205G>C	XP_011522932.1:p.Met735Ile
XM_011524631.1:c.2205G>C	XP_011522933.1:p.Met735Ile
XM_011524632.1:c.1164G>C	XP_011522934.1:p.Val388=
XM_006721823.2:c.2394G>C	XP_006721886.1:p.Val798=
XM_006721824.4:c.2394G>C	XP_006721887.1:p.Val798=
XM_011524628.3:c.2394G>C	XP_011522930.1:p.Val798=
XM_011524629.3:c.2292G>C	XP_011522931.1:p.Val764=
XM_011524630.3:c.2205G>C	XP_011522932.1:p.Met735Ile
XM_011524631.3:c.2205G>C	XP_011522933.1:p.Met735Ile
XM_011524632.3:c.1164G>C	XP_011522934.1:p.Val388=
XM_017024488.2:c.2205G>C	XP_016879977.1:p.Met735Ile
XM_017024489.1:c.2292G>C	XP_016879978.1:p.Val764=
NM_001193466.2:c.2394G>C	NP_001180395.1:p.Val798=
NM_015443.4:c.2394G>C MANE Select	NP_056258.1:p.Val798=
NM_001193465.2:c.2394G>C	NP_001180394.1:p.Val798=
NM_001379198.1:c.2394G>C	NP_001366127.1:p.Val798=