Canonical Allele Identifier: CA408564311

Gene: ASXL1

Linked Data

• dbSNP Id: rs1282636106
• gnomAD v3: 20-32436751-G-A
• gnomAD v4: 20-32436751-G-A
• MyVariant Identifiers: chr20:g.31024554G>A (hg19) ; chr20:g.32436751G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.32436751G>A , CM000682.2:g.32436751G>A	GRCh38
NC_000020.10:g.31024554G>A , CM000682.1:g.31024554G>A	GRCh37
NC_000020.9:g.30488215G>A	NCBI36
NG_027868.1:g.83408G>A , LRG_630:g.83408G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375687.10:c.4039G>A MANE Select	ENSP00000364839.4:p.Gly1347Ser
ENST00000646985.1:c.3856G>A	ENSP00000495053.1:p.Gly1286Ser
ENST00000647223.1:n.6392G>A
ENST00000651418.1:c.1870-1679G>A	ENSP00000499150.1:n.1870-1679G>A
ENST00000306058.9:c.4024G>A	ENSP00000305119.5:p.Gly1342Ser
ENST00000375687.8:c.4039G>A	ENSP00000364839.4:p.Gly1347Ser
ENST00000613218.4:c.4039G>A	ENSP00000480487.1:p.Gly1347Ser
ENST00000620121.4:c.4039G>A	ENSP00000481978.1:p.Gly1347Ser
NM_015338.5:c.4039G>A , LRG_630t1:c.4039G>A	NP_056153.2:p.Gly1347Ser
XM_006723727.2:c.4036G>A	XP_006723790.1:p.Gly1346Ser
XM_006723728.2:c.4009G>A	XP_006723791.1:p.Gly1337Ser
XM_006723730.2:c.3955G>A	XP_006723793.1:p.Gly1319Ser
XM_006723732.2:c.3856G>A	XP_006723795.1:p.Gly1286Ser
XM_006723733.1:c.3355G>A	XP_006723796.1:p.Gly1119Ser
XM_011528647.1:c.4303G>A	XP_011526949.1:p.Gly1435Ser
XM_011528648.1:c.4300G>A	XP_011526950.1:p.Gly1434Ser
XM_011528649.1:c.4219G>A	XP_011526951.1:p.Gly1407Ser
XM_011528650.1:c.4150G>A	XP_011526952.1:p.Gly1384Ser
XM_011528651.1:c.4018G>A	XP_011526953.1:p.Gly1340Ser
XM_011528652.1:c.3955G>A	XP_011526954.1:p.Gly1319Ser
NM_001363734.1:c.3856G>A	NP_001350663.1:p.Gly1286Ser
XM_006723727.3:c.4036G>A	XP_006723790.1:p.Gly1346Ser
XM_006723728.3:c.4009G>A	XP_006723791.1:p.Gly1337Ser
XM_006723730.4:c.3955G>A	XP_006723793.1:p.Gly1319Ser
XM_011528648.3:c.4300G>A	XP_011526950.1:p.Gly1434Ser
XM_011528652.2:c.3955G>A	XP_011526954.1:p.Gly1319Ser
XM_017027704.1:c.3955G>A	XP_016883193.1:p.Gly1319Ser
XM_017027705.1:c.3955G>A	XP_016883194.1:p.Gly1319Ser
XM_017027706.1:c.3886G>A	XP_016883195.1:p.Gly1296Ser
NM_015338.6:c.4039G>A MANE Select	NP_056153.2:p.Gly1347Ser