Canonical Allele Identifier: CA408563328

Gene: ASXL1

Linked Data

• ClinVar Variation Id: 1709430
• ClinVar RCV Id: RCV002289245
• dbSNP Id: rs2145383613
• MyVariant Identifiers: chr20:g.31024080G>A (hg19) ; chr20:g.32436277G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.32436277G>A , CM000682.2:g.32436277G>A	GRCh38
NC_000020.10:g.31024080G>A , CM000682.1:g.31024080G>A	GRCh37
NC_000020.9:g.30487741G>A	NCBI36
NG_027868.1:g.82934G>A , LRG_630:g.82934G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375687.10:c.3565G>A MANE Select	ENSP00000364839.4:p.Ala1189Thr
ENST00000646985.1:c.3382G>A	ENSP00000495053.1:p.Ala1128Thr
ENST00000647223.1:n.5918G>A
ENST00000651418.1:c.1869+1696G>A	ENSP00000499150.1:n.1869+1696G>A
ENST00000306058.9:c.3550G>A	ENSP00000305119.5:p.Ala1184Thr
ENST00000375687.8:c.3565G>A	ENSP00000364839.4:p.Ala1189Thr
ENST00000613218.4:c.3565G>A	ENSP00000480487.1:p.Ala1189Thr
ENST00000620121.4:c.3565G>A	ENSP00000481978.1:p.Ala1189Thr
NM_015338.5:c.3565G>A , LRG_630t1:c.3565G>A	NP_056153.2:p.Ala1189Thr
XM_006723727.2:c.3562G>A	XP_006723790.1:p.Ala1188Thr
XM_006723728.2:c.3535G>A	XP_006723791.1:p.Ala1179Thr
XM_006723730.2:c.3481G>A	XP_006723793.1:p.Ala1161Thr
XM_006723732.2:c.3382G>A	XP_006723795.1:p.Ala1128Thr
XM_006723733.1:c.2881G>A	XP_006723796.1:p.Ala961Thr
XM_011528647.1:c.3829G>A	XP_011526949.1:p.Ala1277Thr
XM_011528648.1:c.3826G>A	XP_011526950.1:p.Ala1276Thr
XM_011528649.1:c.3745G>A	XP_011526951.1:p.Ala1249Thr
XM_011528650.1:c.3676G>A	XP_011526952.1:p.Ala1226Thr
XM_011528651.1:c.3544G>A	XP_011526953.1:p.Ala1182Thr
XM_011528652.1:c.3481G>A	XP_011526954.1:p.Ala1161Thr
NM_001363734.1:c.3382G>A	NP_001350663.1:p.Ala1128Thr
XM_006723727.3:c.3562G>A	XP_006723790.1:p.Ala1188Thr
XM_006723728.3:c.3535G>A	XP_006723791.1:p.Ala1179Thr
XM_006723730.4:c.3481G>A	XP_006723793.1:p.Ala1161Thr
XM_011528648.3:c.3826G>A	XP_011526950.1:p.Ala1276Thr
XM_011528652.2:c.3481G>A	XP_011526954.1:p.Ala1161Thr
XM_017027704.1:c.3481G>A	XP_016883193.1:p.Ala1161Thr
XM_017027705.1:c.3481G>A	XP_016883194.1:p.Ala1161Thr
XM_017027706.1:c.3412G>A	XP_016883195.1:p.Ala1138Thr
NM_015338.6:c.3565G>A MANE Select	NP_056153.2:p.Ala1189Thr