Canonical Allele Identifier: CA408564437

Gene: ASXL1

Linked Data

• dbSNP Id: rs143041800
• MyVariant Identifiers: chr20:g.31024613C>A (hg19) ; chr20:g.32436810C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.32436810C>A , CM000682.2:g.32436810C>A	GRCh38
NC_000020.10:g.31024613C>A , CM000682.1:g.31024613C>A	GRCh37
NC_000020.9:g.30488274C>A	NCBI36
NG_027868.1:g.83467C>A , LRG_630:g.83467C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375687.10:c.4098C>A MANE Select	ENSP00000364839.4:p.Ser1366Arg
ENST00000646985.1:c.3915C>A	ENSP00000495053.1:p.Ser1305Arg
ENST00000647223.1:n.6451C>A
ENST00000651418.1:c.1870-1620C>A	ENSP00000499150.1:n.1870-1620C>A
ENST00000306058.9:c.4083C>A	ENSP00000305119.5:p.Ser1361Arg
ENST00000375687.8:c.4098C>A	ENSP00000364839.4:p.Ser1366Arg
ENST00000613218.4:c.4098C>A	ENSP00000480487.1:p.Ser1366Arg
ENST00000620121.4:c.4098C>A	ENSP00000481978.1:p.Ser1366Arg
NM_015338.5:c.4098C>A , LRG_630t1:c.4098C>A	NP_056153.2:p.Ser1366Arg
XM_006723727.2:c.4095C>A	XP_006723790.1:p.Ser1365Arg
XM_006723728.2:c.4068C>A	XP_006723791.1:p.Ser1356Arg
XM_006723730.2:c.4014C>A	XP_006723793.1:p.Ser1338Arg
XM_006723732.2:c.3915C>A	XP_006723795.1:p.Ser1305Arg
XM_006723733.1:c.3414C>A	XP_006723796.1:p.Ser1138Arg
XM_011528647.1:c.4362C>A	XP_011526949.1:p.Ser1454Arg
XM_011528648.1:c.4359C>A	XP_011526950.1:p.Ser1453Arg
XM_011528649.1:c.4278C>A	XP_011526951.1:p.Ser1426Arg
XM_011528650.1:c.4209C>A	XP_011526952.1:p.Ser1403Arg
XM_011528651.1:c.4077C>A	XP_011526953.1:p.Ser1359Arg
XM_011528652.1:c.4014C>A	XP_011526954.1:p.Ser1338Arg
NM_001363734.1:c.3915C>A	NP_001350663.1:p.Ser1305Arg
XM_006723727.3:c.4095C>A	XP_006723790.1:p.Ser1365Arg
XM_006723728.3:c.4068C>A	XP_006723791.1:p.Ser1356Arg
XM_006723730.4:c.4014C>A	XP_006723793.1:p.Ser1338Arg
XM_011528648.3:c.4359C>A	XP_011526950.1:p.Ser1453Arg
XM_011528652.2:c.4014C>A	XP_011526954.1:p.Ser1338Arg
XM_017027704.1:c.4014C>A	XP_016883193.1:p.Ser1338Arg
XM_017027705.1:c.4014C>A	XP_016883194.1:p.Ser1338Arg
XM_017027706.1:c.3945C>A	XP_016883195.1:p.Ser1315Arg
NM_015338.6:c.4098C>A MANE Select	NP_056153.2:p.Ser1366Arg