Canonical Allele Identifier: CA408564359

Gene: ASXL1

Linked Data

• MyVariant Identifiers: chr20:g.31024578G>A (hg19) ; chr20:g.32436775G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.32436775G>A , CM000682.2:g.32436775G>A	GRCh38
NC_000020.10:g.31024578G>A , CM000682.1:g.31024578G>A	GRCh37
NC_000020.9:g.30488239G>A	NCBI36
NG_027868.1:g.83432G>A , LRG_630:g.83432G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375687.10:c.4063G>A MANE Select	ENSP00000364839.4:p.Asp1355Asn
ENST00000646985.1:c.3880G>A	ENSP00000495053.1:p.Asp1294Asn
ENST00000647223.1:n.6416G>A
ENST00000651418.1:c.1870-1655G>A	ENSP00000499150.1:n.1870-1655G>A
ENST00000306058.9:c.4048G>A	ENSP00000305119.5:p.Asp1350Asn
ENST00000375687.8:c.4063G>A	ENSP00000364839.4:p.Asp1355Asn
ENST00000613218.4:c.4063G>A	ENSP00000480487.1:p.Asp1355Asn
ENST00000620121.4:c.4063G>A	ENSP00000481978.1:p.Asp1355Asn
NM_015338.5:c.4063G>A , LRG_630t1:c.4063G>A	NP_056153.2:p.Asp1355Asn
XM_006723727.2:c.4060G>A	XP_006723790.1:p.Asp1354Asn
XM_006723728.2:c.4033G>A	XP_006723791.1:p.Asp1345Asn
XM_006723730.2:c.3979G>A	XP_006723793.1:p.Asp1327Asn
XM_006723732.2:c.3880G>A	XP_006723795.1:p.Asp1294Asn
XM_006723733.1:c.3379G>A	XP_006723796.1:p.Asp1127Asn
XM_011528647.1:c.4327G>A	XP_011526949.1:p.Asp1443Asn
XM_011528648.1:c.4324G>A	XP_011526950.1:p.Asp1442Asn
XM_011528649.1:c.4243G>A	XP_011526951.1:p.Asp1415Asn
XM_011528650.1:c.4174G>A	XP_011526952.1:p.Asp1392Asn
XM_011528651.1:c.4042G>A	XP_011526953.1:p.Asp1348Asn
XM_011528652.1:c.3979G>A	XP_011526954.1:p.Asp1327Asn
NM_001363734.1:c.3880G>A	NP_001350663.1:p.Asp1294Asn
XM_006723727.3:c.4060G>A	XP_006723790.1:p.Asp1354Asn
XM_006723728.3:c.4033G>A	XP_006723791.1:p.Asp1345Asn
XM_006723730.4:c.3979G>A	XP_006723793.1:p.Asp1327Asn
XM_011528648.3:c.4324G>A	XP_011526950.1:p.Asp1442Asn
XM_011528652.2:c.3979G>A	XP_011526954.1:p.Asp1327Asn
XM_017027704.1:c.3979G>A	XP_016883193.1:p.Asp1327Asn
XM_017027705.1:c.3979G>A	XP_016883194.1:p.Asp1327Asn
XM_017027706.1:c.3910G>A	XP_016883195.1:p.Asp1304Asn
NM_015338.6:c.4063G>A MANE Select	NP_056153.2:p.Asp1355Asn