Canonical Allele Identifier: CA408564129

Gene: ASXL1

Linked Data

• dbSNP Id: rs2145390020
• MyVariant Identifiers: chr20:g.31024465C>A (hg19) ; chr20:g.32436662C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.32436662C>A , CM000682.2:g.32436662C>A	GRCh38
NC_000020.10:g.31024465C>A , CM000682.1:g.31024465C>A	GRCh37
NC_000020.9:g.30488126C>A	NCBI36
NG_027868.1:g.83319C>A , LRG_630:g.83319C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375687.10:c.3950C>A MANE Select	ENSP00000364839.4:p.Pro1317His
ENST00000646985.1:c.3767C>A	ENSP00000495053.1:p.Pro1256His
ENST00000647223.1:n.6303C>A
ENST00000651418.1:c.1870-1768C>A	ENSP00000499150.1:n.1870-1768C>A
ENST00000306058.9:c.3935C>A	ENSP00000305119.5:p.Pro1312His
ENST00000375687.8:c.3950C>A	ENSP00000364839.4:p.Pro1317His
ENST00000613218.4:c.3950C>A	ENSP00000480487.1:p.Pro1317His
ENST00000620121.4:c.3950C>A	ENSP00000481978.1:p.Pro1317His
NM_015338.5:c.3950C>A , LRG_630t1:c.3950C>A	NP_056153.2:p.Pro1317His
XM_006723727.2:c.3947C>A	XP_006723790.1:p.Pro1316His
XM_006723728.2:c.3920C>A	XP_006723791.1:p.Pro1307His
XM_006723730.2:c.3866C>A	XP_006723793.1:p.Pro1289His
XM_006723732.2:c.3767C>A	XP_006723795.1:p.Pro1256His
XM_006723733.1:c.3266C>A	XP_006723796.1:p.Pro1089His
XM_011528647.1:c.4214C>A	XP_011526949.1:p.Pro1405His
XM_011528648.1:c.4211C>A	XP_011526950.1:p.Pro1404His
XM_011528649.1:c.4130C>A	XP_011526951.1:p.Pro1377His
XM_011528650.1:c.4061C>A	XP_011526952.1:p.Pro1354His
XM_011528651.1:c.3929C>A	XP_011526953.1:p.Pro1310His
XM_011528652.1:c.3866C>A	XP_011526954.1:p.Pro1289His
NM_001363734.1:c.3767C>A	NP_001350663.1:p.Pro1256His
XM_006723727.3:c.3947C>A	XP_006723790.1:p.Pro1316His
XM_006723728.3:c.3920C>A	XP_006723791.1:p.Pro1307His
XM_006723730.4:c.3866C>A	XP_006723793.1:p.Pro1289His
XM_011528648.3:c.4211C>A	XP_011526950.1:p.Pro1404His
XM_011528652.2:c.3866C>A	XP_011526954.1:p.Pro1289His
XM_017027704.1:c.3866C>A	XP_016883193.1:p.Pro1289His
XM_017027705.1:c.3866C>A	XP_016883194.1:p.Pro1289His
XM_017027706.1:c.3797C>A	XP_016883195.1:p.Pro1266His
NM_015338.6:c.3950C>A MANE Select	NP_056153.2:p.Pro1317His