Canonical Allele Identifier: CA408564360

Gene: ASXL1

Linked Data

• dbSNP Id: rs897163423
• gnomAD v2: 20-31024578-G-T
• gnomAD v4: 20-32436775-G-T
• MyVariant Identifiers: chr20:g.31024578G>T (hg19) ; chr20:g.32436775G>T (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375687.10:c.4063G>T MANE Select	ENSP00000364839.4:p.Asp1355Tyr
ENST00000646985.1:c.3880G>T	ENSP00000495053.1:p.Asp1294Tyr
ENST00000647223.1:n.6416G>T
ENST00000651418.1:c.1870-1655G>T	ENSP00000499150.1:n.1870-1655G>T
ENST00000306058.9:c.4048G>T	ENSP00000305119.5:p.Asp1350Tyr
ENST00000375687.8:c.4063G>T	ENSP00000364839.4:p.Asp1355Tyr
ENST00000613218.4:c.4063G>T	ENSP00000480487.1:p.Asp1355Tyr
ENST00000620121.4:c.4063G>T	ENSP00000481978.1:p.Asp1355Tyr
NM_015338.5:c.4063G>T , LRG_630t1:c.4063G>T	NP_056153.2:p.Asp1355Tyr
XM_006723727.2:c.4060G>T	XP_006723790.1:p.Asp1354Tyr
XM_006723728.2:c.4033G>T	XP_006723791.1:p.Asp1345Tyr
XM_006723730.2:c.3979G>T	XP_006723793.1:p.Asp1327Tyr
XM_006723732.2:c.3880G>T	XP_006723795.1:p.Asp1294Tyr
XM_006723733.1:c.3379G>T	XP_006723796.1:p.Asp1127Tyr
XM_011528647.1:c.4327G>T	XP_011526949.1:p.Asp1443Tyr
XM_011528648.1:c.4324G>T	XP_011526950.1:p.Asp1442Tyr
XM_011528649.1:c.4243G>T	XP_011526951.1:p.Asp1415Tyr
XM_011528650.1:c.4174G>T	XP_011526952.1:p.Asp1392Tyr
XM_011528651.1:c.4042G>T	XP_011526953.1:p.Asp1348Tyr
XM_011528652.1:c.3979G>T	XP_011526954.1:p.Asp1327Tyr
NM_001363734.1:c.3880G>T	NP_001350663.1:p.Asp1294Tyr
XM_006723727.3:c.4060G>T	XP_006723790.1:p.Asp1354Tyr
XM_006723728.3:c.4033G>T	XP_006723791.1:p.Asp1345Tyr
XM_006723730.4:c.3979G>T	XP_006723793.1:p.Asp1327Tyr
XM_011528648.3:c.4324G>T	XP_011526950.1:p.Asp1442Tyr
XM_011528652.2:c.3979G>T	XP_011526954.1:p.Asp1327Tyr
XM_017027704.1:c.3979G>T	XP_016883193.1:p.Asp1327Tyr
XM_017027705.1:c.3979G>T	XP_016883194.1:p.Asp1327Tyr
XM_017027706.1:c.3910G>T	XP_016883195.1:p.Asp1304Tyr
NM_015338.6:c.4063G>T MANE Select	NP_056153.2:p.Asp1355Tyr