Canonical Allele Identifier: CA408551663

Gene: ASXL1

Linked Data

• MyVariant Identifiers: chr20:g.31016036A>C (hg19) ; chr20:g.32428233A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.32428233A>C , CM000682.2:g.32428233A>C	GRCh38
NC_000020.10:g.31016036A>C , CM000682.1:g.31016036A>C	GRCh37
NC_000020.9:g.30479697A>C	NCBI36
NG_027868.1:g.74890A>C , LRG_630:g.74890A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375687.10:c.358A>C MANE Select	ENSP00000364839.4:p.Ser120Arg
ENST00000470145.3:n.301A>C
ENST00000643168.1:c.274A>C	ENSP00000495003.1:p.Ser92Arg
ENST00000644060.1:n.1162A>C
ENST00000644587.1:c.*197A>C	ENSP00000494813.1:n.*197A>C
ENST00000644615.1:n.62A>C
ENST00000645514.1:n.106A>C
ENST00000646985.1:c.328A>C	ENSP00000495053.1:p.Ser110Arg
ENST00000651418.1:c.358A>C	ENSP00000499150.1:p.Ser120Arg
ENST00000306058.9:c.343A>C	ENSP00000305119.5:p.Ser115Arg
ENST00000375687.8:c.358A>C	ENSP00000364839.4:p.Ser120Arg
ENST00000470145.2:n.301A>C
ENST00000613218.4:c.358A>C	ENSP00000480487.1:p.Ser120Arg
ENST00000620121.4:c.358A>C	ENSP00000481978.1:p.Ser120Arg
NM_015338.5:c.358A>C , LRG_630t1:c.358A>C	NP_056153.2:p.Ser120Arg
XM_006723727.2:c.355A>C	XP_006723790.1:p.Ser119Arg
XM_006723728.2:c.328A>C	XP_006723791.1:p.Ser110Arg
XM_006723730.2:c.274A>C	XP_006723793.1:p.Ser92Arg
XM_006723732.2:c.328A>C	XP_006723795.1:p.Ser110Arg
XM_011528647.1:c.622A>C	XP_011526949.1:p.Ser208Arg
XM_011528648.1:c.619A>C	XP_011526950.1:p.Ser207Arg
XM_011528649.1:c.538A>C	XP_011526951.1:p.Ser180Arg
XM_011528650.1:c.622A>C	XP_011526952.1:p.Ser208Arg
XM_011528651.1:c.337A>C	XP_011526953.1:p.Ser113Arg
XM_011528652.1:c.274A>C	XP_011526954.1:p.Ser92Arg
NM_001363734.1:c.328A>C	NP_001350663.1:p.Ser110Arg
XM_006723727.3:c.355A>C	XP_006723790.1:p.Ser119Arg
XM_006723728.3:c.328A>C	XP_006723791.1:p.Ser110Arg
XM_006723730.4:c.274A>C	XP_006723793.1:p.Ser92Arg
XM_011528648.3:c.619A>C	XP_011526950.1:p.Ser207Arg
XM_011528652.2:c.274A>C	XP_011526954.1:p.Ser92Arg
XM_017027704.1:c.274A>C	XP_016883193.1:p.Ser92Arg
XM_017027705.1:c.274A>C	XP_016883194.1:p.Ser92Arg
XM_017027706.1:c.358A>C	XP_016883195.1:p.Ser120Arg
NM_015338.6:c.358A>C MANE Select	NP_056153.2:p.Ser120Arg