Canonical Allele Identifier: CA408564444
Gene: ASXL1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.32436814A>C , CM000682.2:g.32436814A>C GRCh38
NC_000020.10:g.31024617A>C , CM000682.1:g.31024617A>C GRCh37
NC_000020.9:g.30488278A>C NCBI36
NG_027868.1:g.83471A>C , LRG_630:g.83471A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000375687.10:c.4102A>C MANE Select ENSP00000364839.4:p.Lys1368Gln
ENST00000646985.1:c.3919A>C ENSP00000495053.1:p.Lys1307Gln
ENST00000647223.1:n.6455A>C
ENST00000651418.1:c.1870-1616A>C ENSP00000499150.1:n.1870-1616A>C
ENST00000306058.9:c.4087A>C ENSP00000305119.5:p.Lys1363Gln
ENST00000375687.8:c.4102A>C ENSP00000364839.4:p.Lys1368Gln
ENST00000613218.4:c.4102A>C ENSP00000480487.1:p.Lys1368Gln
ENST00000620121.4:c.4102A>C ENSP00000481978.1:p.Lys1368Gln
NM_015338.5:c.4102A>C , LRG_630t1:c.4102A>C NP_056153.2:p.Lys1368Gln
XM_006723727.2:c.4099A>C XP_006723790.1:p.Lys1367Gln
XM_006723728.2:c.4072A>C XP_006723791.1:p.Lys1358Gln
XM_006723730.2:c.4018A>C XP_006723793.1:p.Lys1340Gln
XM_006723732.2:c.3919A>C XP_006723795.1:p.Lys1307Gln
XM_006723733.1:c.3418A>C XP_006723796.1:p.Lys1140Gln
XM_011528647.1:c.4366A>C XP_011526949.1:p.Lys1456Gln
XM_011528648.1:c.4363A>C XP_011526950.1:p.Lys1455Gln
XM_011528649.1:c.4282A>C XP_011526951.1:p.Lys1428Gln
XM_011528650.1:c.4213A>C XP_011526952.1:p.Lys1405Gln
XM_011528651.1:c.4081A>C XP_011526953.1:p.Lys1361Gln
XM_011528652.1:c.4018A>C XP_011526954.1:p.Lys1340Gln
NM_001363734.1:c.3919A>C NP_001350663.1:p.Lys1307Gln
XM_006723727.3:c.4099A>C XP_006723790.1:p.Lys1367Gln
XM_006723728.3:c.4072A>C XP_006723791.1:p.Lys1358Gln
XM_006723730.4:c.4018A>C XP_006723793.1:p.Lys1340Gln
XM_011528648.3:c.4363A>C XP_011526950.1:p.Lys1455Gln
XM_011528652.2:c.4018A>C XP_011526954.1:p.Lys1340Gln
XM_017027704.1:c.4018A>C XP_016883193.1:p.Lys1340Gln
XM_017027705.1:c.4018A>C XP_016883194.1:p.Lys1340Gln
XM_017027706.1:c.3949A>C XP_016883195.1:p.Lys1317Gln
NM_015338.6:c.4102A>C MANE Select NP_056153.2:p.Lys1368Gln