Canonical Allele Identifier: CA408564367

Gene: ASXL1

Linked Data

• dbSNP Id: rs2145391756
• MyVariant Identifiers: chr20:g.31024581T>G (hg19) ; chr20:g.32436778T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.32436778T>G , CM000682.2:g.32436778T>G	GRCh38
NC_000020.10:g.31024581T>G , CM000682.1:g.31024581T>G	GRCh37
NC_000020.9:g.30488242T>G	NCBI36
NG_027868.1:g.83435T>G , LRG_630:g.83435T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375687.10:c.4066T>G MANE Select	ENSP00000364839.4:p.Trp1356Gly
ENST00000646985.1:c.3883T>G	ENSP00000495053.1:p.Trp1295Gly
ENST00000647223.1:n.6419T>G
ENST00000651418.1:c.1870-1652T>G	ENSP00000499150.1:n.1870-1652T>G
ENST00000306058.9:c.4051T>G	ENSP00000305119.5:p.Trp1351Gly
ENST00000375687.8:c.4066T>G	ENSP00000364839.4:p.Trp1356Gly
ENST00000613218.4:c.4066T>G	ENSP00000480487.1:p.Trp1356Gly
ENST00000620121.4:c.4066T>G	ENSP00000481978.1:p.Trp1356Gly
NM_015338.5:c.4066T>G , LRG_630t1:c.4066T>G	NP_056153.2:p.Trp1356Gly
XM_006723727.2:c.4063T>G	XP_006723790.1:p.Trp1355Gly
XM_006723728.2:c.4036T>G	XP_006723791.1:p.Trp1346Gly
XM_006723730.2:c.3982T>G	XP_006723793.1:p.Trp1328Gly
XM_006723732.2:c.3883T>G	XP_006723795.1:p.Trp1295Gly
XM_006723733.1:c.3382T>G	XP_006723796.1:p.Trp1128Gly
XM_011528647.1:c.4330T>G	XP_011526949.1:p.Trp1444Gly
XM_011528648.1:c.4327T>G	XP_011526950.1:p.Trp1443Gly
XM_011528649.1:c.4246T>G	XP_011526951.1:p.Trp1416Gly
XM_011528650.1:c.4177T>G	XP_011526952.1:p.Trp1393Gly
XM_011528651.1:c.4045T>G	XP_011526953.1:p.Trp1349Gly
XM_011528652.1:c.3982T>G	XP_011526954.1:p.Trp1328Gly
NM_001363734.1:c.3883T>G	NP_001350663.1:p.Trp1295Gly
XM_006723727.3:c.4063T>G	XP_006723790.1:p.Trp1355Gly
XM_006723728.3:c.4036T>G	XP_006723791.1:p.Trp1346Gly
XM_006723730.4:c.3982T>G	XP_006723793.1:p.Trp1328Gly
XM_011528648.3:c.4327T>G	XP_011526950.1:p.Trp1443Gly
XM_011528652.2:c.3982T>G	XP_011526954.1:p.Trp1328Gly
XM_017027704.1:c.3982T>G	XP_016883193.1:p.Trp1328Gly
XM_017027705.1:c.3982T>G	XP_016883194.1:p.Trp1328Gly
XM_017027706.1:c.3913T>G	XP_016883195.1:p.Trp1305Gly
NM_015338.6:c.4066T>G MANE Select	NP_056153.2:p.Trp1356Gly