Canonical Allele Identifier: CA408564139

Gene: ASXL1

Linked Data

• MyVariant Identifiers: chr20:g.31024470C>G (hg19) ; chr20:g.32436667C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.32436667C>G , CM000682.2:g.32436667C>G	GRCh38
NC_000020.10:g.31024470C>G , CM000682.1:g.31024470C>G	GRCh37
NC_000020.9:g.30488131C>G	NCBI36
NG_027868.1:g.83324C>G , LRG_630:g.83324C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375687.10:c.3955C>G MANE Select	ENSP00000364839.4:p.Pro1319Ala
ENST00000646985.1:c.3772C>G	ENSP00000495053.1:p.Pro1258Ala
ENST00000647223.1:n.6308C>G
ENST00000651418.1:c.1870-1763C>G	ENSP00000499150.1:n.1870-1763C>G
ENST00000306058.9:c.3940C>G	ENSP00000305119.5:p.Pro1314Ala
ENST00000375687.8:c.3955C>G	ENSP00000364839.4:p.Pro1319Ala
ENST00000613218.4:c.3955C>G	ENSP00000480487.1:p.Pro1319Ala
ENST00000620121.4:c.3955C>G	ENSP00000481978.1:p.Pro1319Ala
NM_015338.5:c.3955C>G , LRG_630t1:c.3955C>G	NP_056153.2:p.Pro1319Ala
XM_006723727.2:c.3952C>G	XP_006723790.1:p.Pro1318Ala
XM_006723728.2:c.3925C>G	XP_006723791.1:p.Pro1309Ala
XM_006723730.2:c.3871C>G	XP_006723793.1:p.Pro1291Ala
XM_006723732.2:c.3772C>G	XP_006723795.1:p.Pro1258Ala
XM_006723733.1:c.3271C>G	XP_006723796.1:p.Pro1091Ala
XM_011528647.1:c.4219C>G	XP_011526949.1:p.Pro1407Ala
XM_011528648.1:c.4216C>G	XP_011526950.1:p.Pro1406Ala
XM_011528649.1:c.4135C>G	XP_011526951.1:p.Pro1379Ala
XM_011528650.1:c.4066C>G	XP_011526952.1:p.Pro1356Ala
XM_011528651.1:c.3934C>G	XP_011526953.1:p.Pro1312Ala
XM_011528652.1:c.3871C>G	XP_011526954.1:p.Pro1291Ala
NM_001363734.1:c.3772C>G	NP_001350663.1:p.Pro1258Ala
XM_006723727.3:c.3952C>G	XP_006723790.1:p.Pro1318Ala
XM_006723728.3:c.3925C>G	XP_006723791.1:p.Pro1309Ala
XM_006723730.4:c.3871C>G	XP_006723793.1:p.Pro1291Ala
XM_011528648.3:c.4216C>G	XP_011526950.1:p.Pro1406Ala
XM_011528652.2:c.3871C>G	XP_011526954.1:p.Pro1291Ala
XM_017027704.1:c.3871C>G	XP_016883193.1:p.Pro1291Ala
XM_017027705.1:c.3871C>G	XP_016883194.1:p.Pro1291Ala
XM_017027706.1:c.3802C>G	XP_016883195.1:p.Pro1268Ala
NM_015338.6:c.3955C>G MANE Select	NP_056153.2:p.Pro1319Ala