Canonical Allele Identifier: CA500372069

Gene: KANSL1

Linked Data

• MyVariant Identifiers: chr17:g.44109638T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.46032272T>G , CM000679.2:g.46032272T>G	GRCh38
NC_000017.10:g.44109638T>G , CM000679.1:g.44109638T>G	GRCh37
NC_000017.9:g.41465485T>G	NCBI36
NG_032784.1:g.198103A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000432791.7:c.2865A>C MANE Select	ENSP00000387393.3:p.Thr955=
ENST00000572904.6:c.2865A>C	ENSP00000461484.1:p.Thr955=
ENST00000574590.6:c.2862A>C	ENSP00000461812.2:p.Thr954=
ENST00000575318.6:c.2673A>C	ENSP00000461299.1:p.Thr891=
ENST00000638275.1:c.2673A>C	ENSP00000492576.1:p.Thr891=
ENST00000638291.1:n.693A>C
ENST00000638551.1:n.813A>C
ENST00000639467.1:c.522A>C	ENSP00000492741.1:p.Thr174=
ENST00000639531.1:c.2676A>C	ENSP00000491765.1:p.Thr892=
ENST00000639805.1:n.282A>C
ENST00000640751.1:n.460A>C
ENST00000648792.1:c.2838-105A>C	ENSP00000497628.1:n.2838-105A>C
ENST00000262419.10:c.2865A>C	ENSP00000262419.6:p.Thr955=
ENST00000432791.5:c.2862A>C	ENSP00000387393.2:p.Thr954=
ENST00000572218.5:n.7082A>C
ENST00000572904.5:c.2865A>C	ENSP00000461484.1:p.Thr955=
ENST00000573682.1:n.251A>C
ENST00000574590.5:c.2865A>C	ENSP00000461812.1:p.Thr955=
ENST00000574963.1:n.295A>C
ENST00000575318.5:c.2673A>C	ENSP00000461299.1:p.Thr891=
ENST00000576870.5:n.837A>C
NM_001193465.1:c.2862A>C	NP_001180394.1:p.Thr954=
NM_001193466.1:c.2865A>C	NP_001180395.1:p.Thr955=
NM_015443.3:c.2865A>C	NP_056258.1:p.Thr955=
XM_006721823.1:c.2865A>C	XP_006721886.1:p.Thr955=
XM_006721824.2:c.2865A>C	XP_006721887.1:p.Thr955=
XM_011524628.1:c.2862A>C	XP_011522930.1:p.Thr954=
XM_011524629.1:c.2763A>C	XP_011522931.1:p.Thr921=
XM_011524630.1:c.2676A>C	XP_011522932.1:p.Thr892=
XM_011524631.1:c.2673A>C	XP_011522933.1:p.Thr891=
XM_011524632.1:c.1635A>C	XP_011522934.1:p.Thr545=
XM_006721823.2:c.2865A>C	XP_006721886.1:p.Thr955=
XM_006721824.4:c.2865A>C	XP_006721887.1:p.Thr955=
XM_011524628.3:c.2862A>C	XP_011522930.1:p.Thr954=
XM_011524629.3:c.2763A>C	XP_011522931.1:p.Thr921=
XM_011524630.3:c.2676A>C	XP_011522932.1:p.Thr892=
XM_011524631.3:c.2673A>C	XP_011522933.1:p.Thr891=
XM_011524632.3:c.1635A>C	XP_011522934.1:p.Thr545=
XM_017024488.2:c.2673A>C	XP_016879977.1:p.Thr891=
NM_001193466.2:c.2865A>C	NP_001180395.1:p.Thr955=
NM_015443.4:c.2865A>C MANE Select	NP_056258.1:p.Thr955=
NM_001193465.2:c.2862A>C	NP_001180394.1:p.Thr954=
NM_001379198.1:c.2865A>C	NP_001366127.1:p.Thr955=