Canonical Allele Identifier: CA408564087
Gene: ASXL1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.32436639T>G , CM000682.2:g.32436639T>G GRCh38
NC_000020.10:g.31024442T>G , CM000682.1:g.31024442T>G GRCh37
NC_000020.9:g.30488103T>G NCBI36
NG_027868.1:g.83296T>G , LRG_630:g.83296T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000375687.10:c.3927T>G MANE Select ENSP00000364839.4:p.Asn1309Lys
ENST00000646985.1:c.3744T>G ENSP00000495053.1:p.Asn1248Lys
ENST00000647223.1:n.6280T>G
ENST00000651418.1:c.1870-1791T>G ENSP00000499150.1:n.1870-1791T>G
ENST00000306058.9:c.3912T>G ENSP00000305119.5:p.Asn1304Lys
ENST00000375687.8:c.3927T>G ENSP00000364839.4:p.Asn1309Lys
ENST00000613218.4:c.3927T>G ENSP00000480487.1:p.Asn1309Lys
ENST00000620121.4:c.3927T>G ENSP00000481978.1:p.Asn1309Lys
NM_015338.5:c.3927T>G , LRG_630t1:c.3927T>G NP_056153.2:p.Asn1309Lys
XM_006723727.2:c.3924T>G XP_006723790.1:p.Asn1308Lys
XM_006723728.2:c.3897T>G XP_006723791.1:p.Asn1299Lys
XM_006723730.2:c.3843T>G XP_006723793.1:p.Asn1281Lys
XM_006723732.2:c.3744T>G XP_006723795.1:p.Asn1248Lys
XM_006723733.1:c.3243T>G XP_006723796.1:p.Asn1081Lys
XM_011528647.1:c.4191T>G XP_011526949.1:p.Asn1397Lys
XM_011528648.1:c.4188T>G XP_011526950.1:p.Asn1396Lys
XM_011528649.1:c.4107T>G XP_011526951.1:p.Asn1369Lys
XM_011528650.1:c.4038T>G XP_011526952.1:p.Asn1346Lys
XM_011528651.1:c.3906T>G XP_011526953.1:p.Asn1302Lys
XM_011528652.1:c.3843T>G XP_011526954.1:p.Asn1281Lys
NM_001363734.1:c.3744T>G NP_001350663.1:p.Asn1248Lys
XM_006723727.3:c.3924T>G XP_006723790.1:p.Asn1308Lys
XM_006723728.3:c.3897T>G XP_006723791.1:p.Asn1299Lys
XM_006723730.4:c.3843T>G XP_006723793.1:p.Asn1281Lys
XM_011528648.3:c.4188T>G XP_011526950.1:p.Asn1396Lys
XM_011528652.2:c.3843T>G XP_011526954.1:p.Asn1281Lys
XM_017027704.1:c.3843T>G XP_016883193.1:p.Asn1281Lys
XM_017027705.1:c.3843T>G XP_016883194.1:p.Asn1281Lys
XM_017027706.1:c.3774T>G XP_016883195.1:p.Asn1258Lys
NM_015338.6:c.3927T>G MANE Select NP_056153.2:p.Asn1309Lys