Canonical Allele Identifier: CA408564369

Gene: ASXL1

Linked Data

• MyVariant Identifiers: chr20:g.31024582G>C (hg19) ; chr20:g.32436779G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.32436779G>C , CM000682.2:g.32436779G>C	GRCh38
NC_000020.10:g.31024582G>C , CM000682.1:g.31024582G>C	GRCh37
NC_000020.9:g.30488243G>C	NCBI36
NG_027868.1:g.83436G>C , LRG_630:g.83436G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375687.10:c.4067G>C MANE Select	ENSP00000364839.4:p.Trp1356Ser
ENST00000646985.1:c.3884G>C	ENSP00000495053.1:p.Trp1295Ser
ENST00000647223.1:n.6420G>C
ENST00000651418.1:c.1870-1651G>C	ENSP00000499150.1:n.1870-1651G>C
ENST00000306058.9:c.4052G>C	ENSP00000305119.5:p.Trp1351Ser
ENST00000375687.8:c.4067G>C	ENSP00000364839.4:p.Trp1356Ser
ENST00000613218.4:c.4067G>C	ENSP00000480487.1:p.Trp1356Ser
ENST00000620121.4:c.4067G>C	ENSP00000481978.1:p.Trp1356Ser
NM_015338.5:c.4067G>C , LRG_630t1:c.4067G>C	NP_056153.2:p.Trp1356Ser
XM_006723727.2:c.4064G>C	XP_006723790.1:p.Trp1355Ser
XM_006723728.2:c.4037G>C	XP_006723791.1:p.Trp1346Ser
XM_006723730.2:c.3983G>C	XP_006723793.1:p.Trp1328Ser
XM_006723732.2:c.3884G>C	XP_006723795.1:p.Trp1295Ser
XM_006723733.1:c.3383G>C	XP_006723796.1:p.Trp1128Ser
XM_011528647.1:c.4331G>C	XP_011526949.1:p.Trp1444Ser
XM_011528648.1:c.4328G>C	XP_011526950.1:p.Trp1443Ser
XM_011528649.1:c.4247G>C	XP_011526951.1:p.Trp1416Ser
XM_011528650.1:c.4178G>C	XP_011526952.1:p.Trp1393Ser
XM_011528651.1:c.4046G>C	XP_011526953.1:p.Trp1349Ser
XM_011528652.1:c.3983G>C	XP_011526954.1:p.Trp1328Ser
NM_001363734.1:c.3884G>C	NP_001350663.1:p.Trp1295Ser
XM_006723727.3:c.4064G>C	XP_006723790.1:p.Trp1355Ser
XM_006723728.3:c.4037G>C	XP_006723791.1:p.Trp1346Ser
XM_006723730.4:c.3983G>C	XP_006723793.1:p.Trp1328Ser
XM_011528648.3:c.4328G>C	XP_011526950.1:p.Trp1443Ser
XM_011528652.2:c.3983G>C	XP_011526954.1:p.Trp1328Ser
XM_017027704.1:c.3983G>C	XP_016883193.1:p.Trp1328Ser
XM_017027705.1:c.3983G>C	XP_016883194.1:p.Trp1328Ser
XM_017027706.1:c.3914G>C	XP_016883195.1:p.Trp1305Ser
NM_015338.6:c.4067G>C MANE Select	NP_056153.2:p.Trp1356Ser