Canonical Allele Identifier: CA408564062
Gene: ASXL1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.32436627T>A , CM000682.2:g.32436627T>A GRCh38
NC_000020.10:g.31024430T>A , CM000682.1:g.31024430T>A GRCh37
NC_000020.9:g.30488091T>A NCBI36
NG_027868.1:g.83284T>A , LRG_630:g.83284T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000375687.10:c.3915T>A MANE Select ENSP00000364839.4:p.Phe1305Leu
ENST00000646985.1:c.3732T>A ENSP00000495053.1:p.Phe1244Leu
ENST00000647223.1:n.6268T>A
ENST00000651418.1:c.1870-1803T>A ENSP00000499150.1:n.1870-1803T>A
ENST00000306058.9:c.3900T>A ENSP00000305119.5:p.Phe1300Leu
ENST00000375687.8:c.3915T>A ENSP00000364839.4:p.Phe1305Leu
ENST00000613218.4:c.3915T>A ENSP00000480487.1:p.Phe1305Leu
ENST00000620121.4:c.3915T>A ENSP00000481978.1:p.Phe1305Leu
NM_015338.5:c.3915T>A , LRG_630t1:c.3915T>A NP_056153.2:p.Phe1305Leu
XM_006723727.2:c.3912T>A XP_006723790.1:p.Phe1304Leu
XM_006723728.2:c.3885T>A XP_006723791.1:p.Phe1295Leu
XM_006723730.2:c.3831T>A XP_006723793.1:p.Phe1277Leu
XM_006723732.2:c.3732T>A XP_006723795.1:p.Phe1244Leu
XM_006723733.1:c.3231T>A XP_006723796.1:p.Phe1077Leu
XM_011528647.1:c.4179T>A XP_011526949.1:p.Phe1393Leu
XM_011528648.1:c.4176T>A XP_011526950.1:p.Phe1392Leu
XM_011528649.1:c.4095T>A XP_011526951.1:p.Phe1365Leu
XM_011528650.1:c.4026T>A XP_011526952.1:p.Phe1342Leu
XM_011528651.1:c.3894T>A XP_011526953.1:p.Phe1298Leu
XM_011528652.1:c.3831T>A XP_011526954.1:p.Phe1277Leu
NM_001363734.1:c.3732T>A NP_001350663.1:p.Phe1244Leu
XM_006723727.3:c.3912T>A XP_006723790.1:p.Phe1304Leu
XM_006723728.3:c.3885T>A XP_006723791.1:p.Phe1295Leu
XM_006723730.4:c.3831T>A XP_006723793.1:p.Phe1277Leu
XM_011528648.3:c.4176T>A XP_011526950.1:p.Phe1392Leu
XM_011528652.2:c.3831T>A XP_011526954.1:p.Phe1277Leu
XM_017027704.1:c.3831T>A XP_016883193.1:p.Phe1277Leu
XM_017027705.1:c.3831T>A XP_016883194.1:p.Phe1277Leu
XM_017027706.1:c.3762T>A XP_016883195.1:p.Phe1254Leu
NM_015338.6:c.3915T>A MANE Select NP_056153.2:p.Phe1305Leu