Canonical Allele Identifier: CA500369729

Gene: KANSL1

Linked Data

• MyVariant Identifiers: chr17:g.44115919A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.46038553A>G , CM000679.2:g.46038553A>G	GRCh38
NC_000017.10:g.44115919A>G , CM000679.1:g.44115919A>G	GRCh37
NC_000017.9:g.41471766A>G	NCBI36
NG_032784.1:g.191822T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000432791.7:c.2526T>C MANE Select	ENSP00000387393.3:p.Val842=
ENST00000572904.6:c.2526T>C	ENSP00000461484.1:p.Val842=
ENST00000573286.2:n.4209T>C
ENST00000574590.6:c.2526T>C	ENSP00000461812.2:p.Val842=
ENST00000575318.6:c.2337T>C	ENSP00000461299.1:p.Val779=
ENST00000576137.2:n.523T>C
ENST00000638275.1:c.2337T>C	ENSP00000492576.1:p.Val779=
ENST00000639150.1:c.1260T>C	ENSP00000491906.1:p.Val420=
ENST00000639467.1:c.189T>C	ENSP00000492741.1:p.Val63=
ENST00000639531.1:c.2337T>C	ENSP00000491765.1:p.Val779=
ENST00000640636.1:c.479T>C
ENST00000648792.1:c.2526T>C	ENSP00000497628.1:p.Val842=
ENST00000262419.10:c.2526T>C	ENSP00000262419.6:p.Val842=
ENST00000432791.5:c.2526T>C	ENSP00000387393.2:p.Val842=
ENST00000572218.5:n.6743T>C
ENST00000572904.5:c.2526T>C	ENSP00000461484.1:p.Val842=
ENST00000573286.1:n.382T>C
ENST00000574590.5:c.2526T>C	ENSP00000461812.1:p.Val842=
ENST00000575318.5:c.2337T>C	ENSP00000461299.1:p.Val779=
ENST00000576137.1:n.165T>C
ENST00000576870.5:n.498T>C
NM_001193465.1:c.2526T>C	NP_001180394.1:p.Val842=
NM_001193466.1:c.2526T>C	NP_001180395.1:p.Val842=
NM_015443.3:c.2526T>C	NP_056258.1:p.Val842=
XM_006721823.1:c.2526T>C	XP_006721886.1:p.Val842=
XM_006721824.2:c.2526T>C	XP_006721887.1:p.Val842=
XM_011524628.1:c.2526T>C	XP_011522930.1:p.Val842=
XM_011524629.1:c.2424T>C	XP_011522931.1:p.Val808=
XM_011524630.1:c.2337T>C	XP_011522932.1:p.Val779=
XM_011524631.1:c.2337T>C	XP_011522933.1:p.Val779=
XM_011524632.1:c.1296T>C	XP_011522934.1:p.Val432=
XM_006721823.2:c.2526T>C	XP_006721886.1:p.Val842=
XM_006721824.4:c.2526T>C	XP_006721887.1:p.Val842=
XM_011524628.3:c.2526T>C	XP_011522930.1:p.Val842=
XM_011524629.3:c.2424T>C	XP_011522931.1:p.Val808=
XM_011524630.3:c.2337T>C	XP_011522932.1:p.Val779=
XM_011524631.3:c.2337T>C	XP_011522933.1:p.Val779=
XM_011524632.3:c.1296T>C	XP_011522934.1:p.Val432=
XM_017024488.2:c.2337T>C	XP_016879977.1:p.Val779=
XM_017024489.1:c.2424T>C	XP_016879978.1:p.Val808=
NM_001193466.2:c.2526T>C	NP_001180395.1:p.Val842=
NM_015443.4:c.2526T>C MANE Select	NP_056258.1:p.Val842=
NM_001193465.2:c.2526T>C	NP_001180394.1:p.Val842=
NM_001379198.1:c.2526T>C	NP_001366127.1:p.Val842=