Canonical Allele Identifier: CA408563499

Gene: ASXL1

Linked Data

• gnomAD v4: 20-32436358-G-A
• MyVariant Identifiers: chr20:g.31024161G>A (hg19) ; chr20:g.32436358G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.32436358G>A , CM000682.2:g.32436358G>A	GRCh38
NC_000020.10:g.31024161G>A , CM000682.1:g.31024161G>A	GRCh37
NC_000020.9:g.30487822G>A	NCBI36
NG_027868.1:g.83015G>A , LRG_630:g.83015G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000375687.10:c.3646G>A MANE Select	ENSP00000364839.4:p.Val1216Met
ENST00000646985.1:c.3463G>A	ENSP00000495053.1:p.Val1155Met
ENST00000647223.1:n.5999G>A
ENST00000651418.1:c.1869+1777G>A	ENSP00000499150.1:n.1869+1777G>A
ENST00000306058.9:c.3631G>A	ENSP00000305119.5:p.Val1211Met
ENST00000375687.8:c.3646G>A	ENSP00000364839.4:p.Val1216Met
ENST00000613218.4:c.3646G>A	ENSP00000480487.1:p.Val1216Met
ENST00000620121.4:c.3646G>A	ENSP00000481978.1:p.Val1216Met
NM_015338.5:c.3646G>A , LRG_630t1:c.3646G>A	NP_056153.2:p.Val1216Met
XM_006723727.2:c.3643G>A	XP_006723790.1:p.Val1215Met
XM_006723728.2:c.3616G>A	XP_006723791.1:p.Val1206Met
XM_006723730.2:c.3562G>A	XP_006723793.1:p.Val1188Met
XM_006723732.2:c.3463G>A	XP_006723795.1:p.Val1155Met
XM_006723733.1:c.2962G>A	XP_006723796.1:p.Val988Met
XM_011528647.1:c.3910G>A	XP_011526949.1:p.Val1304Met
XM_011528648.1:c.3907G>A	XP_011526950.1:p.Val1303Met
XM_011528649.1:c.3826G>A	XP_011526951.1:p.Val1276Met
XM_011528650.1:c.3757G>A	XP_011526952.1:p.Val1253Met
XM_011528651.1:c.3625G>A	XP_011526953.1:p.Val1209Met
XM_011528652.1:c.3562G>A	XP_011526954.1:p.Val1188Met
NM_001363734.1:c.3463G>A	NP_001350663.1:p.Val1155Met
XM_006723727.3:c.3643G>A	XP_006723790.1:p.Val1215Met
XM_006723728.3:c.3616G>A	XP_006723791.1:p.Val1206Met
XM_006723730.4:c.3562G>A	XP_006723793.1:p.Val1188Met
XM_011528648.3:c.3907G>A	XP_011526950.1:p.Val1303Met
XM_011528652.2:c.3562G>A	XP_011526954.1:p.Val1188Met
XM_017027704.1:c.3562G>A	XP_016883193.1:p.Val1188Met
XM_017027705.1:c.3562G>A	XP_016883194.1:p.Val1188Met
XM_017027706.1:c.3493G>A	XP_016883195.1:p.Val1165Met
NM_015338.6:c.3646G>A MANE Select	NP_056153.2:p.Val1216Met