Canonical Allele Identifier: CA510467617

Gene: ASXL1

Linked Data

• gnomAD v4: 20-32436756-G-T
• MyVariant Identifiers: chr20:g.31024559G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.32436756G>T , CM000682.2:g.32436756G>T	GRCh38
NC_000020.10:g.31024559G>T , CM000682.1:g.31024559G>T	GRCh37
NC_000020.9:g.30488220G>T	NCBI36
NG_027868.1:g.83413G>T , LRG_630:g.83413G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375687.10:c.4044G>T MANE Select	ENSP00000364839.4:p.Gly1348=
ENST00000646985.1:c.3861G>T	ENSP00000495053.1:p.Gly1287=
ENST00000647223.1:n.6397G>T
ENST00000651418.1:c.1870-1674G>T	ENSP00000499150.1:n.1870-1674G>T
ENST00000306058.9:c.4029G>T	ENSP00000305119.5:p.Gly1343=
ENST00000375687.8:c.4044G>T	ENSP00000364839.4:p.Gly1348=
ENST00000613218.4:c.4044G>T	ENSP00000480487.1:p.Gly1348=
ENST00000620121.4:c.4044G>T	ENSP00000481978.1:p.Gly1348=
NM_015338.5:c.4044G>T , LRG_630t1:c.4044G>T	NP_056153.2:p.Gly1348=
XM_006723727.2:c.4041G>T	XP_006723790.1:p.Gly1347=
XM_006723728.2:c.4014G>T	XP_006723791.1:p.Gly1338=
XM_006723730.2:c.3960G>T	XP_006723793.1:p.Gly1320=
XM_006723732.2:c.3861G>T	XP_006723795.1:p.Gly1287=
XM_006723733.1:c.3360G>T	XP_006723796.1:p.Gly1120=
XM_011528647.1:c.4308G>T	XP_011526949.1:p.Gly1436=
XM_011528648.1:c.4305G>T	XP_011526950.1:p.Gly1435=
XM_011528649.1:c.4224G>T	XP_011526951.1:p.Gly1408=
XM_011528650.1:c.4155G>T	XP_011526952.1:p.Gly1385=
XM_011528651.1:c.4023G>T	XP_011526953.1:p.Gly1341=
XM_011528652.1:c.3960G>T	XP_011526954.1:p.Gly1320=
NM_001363734.1:c.3861G>T	NP_001350663.1:p.Gly1287=
XM_006723727.3:c.4041G>T	XP_006723790.1:p.Gly1347=
XM_006723728.3:c.4014G>T	XP_006723791.1:p.Gly1338=
XM_006723730.4:c.3960G>T	XP_006723793.1:p.Gly1320=
XM_011528648.3:c.4305G>T	XP_011526950.1:p.Gly1435=
XM_011528652.2:c.3960G>T	XP_011526954.1:p.Gly1320=
XM_017027704.1:c.3960G>T	XP_016883193.1:p.Gly1320=
XM_017027705.1:c.3960G>T	XP_016883194.1:p.Gly1320=
XM_017027706.1:c.3891G>T	XP_016883195.1:p.Gly1297=
NM_015338.6:c.4044G>T MANE Select	NP_056153.2:p.Gly1348=