Canonical Allele Identifier: CA408563955

Gene: ASXL1

Linked Data

• dbSNP Id: rs1396654725
• COSMIC: COSM1155720
• MyVariant Identifiers: chr20:g.31024378G>A (hg19) ; chr20:g.32436575G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.32436575G>A , CM000682.2:g.32436575G>A	GRCh38
NC_000020.10:g.31024378G>A , CM000682.1:g.31024378G>A	GRCh37
NC_000020.9:g.30488039G>A	NCBI36
NG_027868.1:g.83232G>A , LRG_630:g.83232G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375687.10:c.3863G>A MANE Select	ENSP00000364839.4:p.Gly1288Asp
ENST00000646985.1:c.3680G>A	ENSP00000495053.1:p.Gly1227Asp
ENST00000647223.1:n.6216G>A
ENST00000651418.1:c.1870-1855G>A	ENSP00000499150.1:n.1870-1855G>A
ENST00000306058.9:c.3848G>A	ENSP00000305119.5:p.Gly1283Asp
ENST00000375687.8:c.3863G>A	ENSP00000364839.4:p.Gly1288Asp
ENST00000613218.4:c.3863G>A	ENSP00000480487.1:p.Gly1288Asp
ENST00000620121.4:c.3863G>A	ENSP00000481978.1:p.Gly1288Asp
NM_015338.5:c.3863G>A , LRG_630t1:c.3863G>A	NP_056153.2:p.Gly1288Asp
XM_006723727.2:c.3860G>A	XP_006723790.1:p.Gly1287Asp
XM_006723728.2:c.3833G>A	XP_006723791.1:p.Gly1278Asp
XM_006723730.2:c.3779G>A	XP_006723793.1:p.Gly1260Asp
XM_006723732.2:c.3680G>A	XP_006723795.1:p.Gly1227Asp
XM_006723733.1:c.3179G>A	XP_006723796.1:p.Gly1060Asp
XM_011528647.1:c.4127G>A	XP_011526949.1:p.Gly1376Asp
XM_011528648.1:c.4124G>A	XP_011526950.1:p.Gly1375Asp
XM_011528649.1:c.4043G>A	XP_011526951.1:p.Gly1348Asp
XM_011528650.1:c.3974G>A	XP_011526952.1:p.Gly1325Asp
XM_011528651.1:c.3842G>A	XP_011526953.1:p.Gly1281Asp
XM_011528652.1:c.3779G>A	XP_011526954.1:p.Gly1260Asp
NM_001363734.1:c.3680G>A	NP_001350663.1:p.Gly1227Asp
XM_006723727.3:c.3860G>A	XP_006723790.1:p.Gly1287Asp
XM_006723728.3:c.3833G>A	XP_006723791.1:p.Gly1278Asp
XM_006723730.4:c.3779G>A	XP_006723793.1:p.Gly1260Asp
XM_011528648.3:c.4124G>A	XP_011526950.1:p.Gly1375Asp
XM_011528652.2:c.3779G>A	XP_011526954.1:p.Gly1260Asp
XM_017027704.1:c.3779G>A	XP_016883193.1:p.Gly1260Asp
XM_017027705.1:c.3779G>A	XP_016883194.1:p.Gly1260Asp
XM_017027706.1:c.3710G>A	XP_016883195.1:p.Gly1237Asp
NM_015338.6:c.3863G>A MANE Select	NP_056153.2:p.Gly1288Asp