Canonical Allele Identifier: CA408551364
Gene: ASXL1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.32428153A>T , CM000682.2:g.32428153A>T GRCh38
NC_000020.10:g.31015956A>T , CM000682.1:g.31015956A>T GRCh37
NC_000020.9:g.30479617A>T NCBI36
NG_027868.1:g.74810A>T , LRG_630:g.74810A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000375687.10:c.278A>T MANE Select ENSP00000364839.4:p.His93Leu
ENST00000470145.3:n.221A>T
ENST00000643168.1:c.194A>T ENSP00000495003.1:p.His65Leu
ENST00000644060.1:n.1082A>T
ENST00000644587.1:c.*117A>T ENSP00000494813.1:n.*117A>T
ENST00000645514.1:n.26A>T
ENST00000645688.1:c.194A>T ENSP00000495488.1:p.His65Leu
ENST00000646985.1:c.248A>T ENSP00000495053.1:p.His83Leu
ENST00000651418.1:c.278A>T ENSP00000499150.1:p.His93Leu
ENST00000306058.9:c.263A>T ENSP00000305119.5:p.His88Leu
ENST00000375687.8:c.278A>T ENSP00000364839.4:p.His93Leu
ENST00000470145.2:n.221A>T
ENST00000613218.4:c.278A>T ENSP00000480487.1:p.His93Leu
ENST00000620121.4:c.278A>T ENSP00000481978.1:p.His93Leu
NM_015338.5:c.278A>T , LRG_630t1:c.278A>T NP_056153.2:p.His93Leu
XM_006723727.2:c.275A>T XP_006723790.1:p.His92Leu
XM_006723728.2:c.248A>T XP_006723791.1:p.His83Leu
XM_006723730.2:c.194A>T XP_006723793.1:p.His65Leu
XM_006723732.2:c.248A>T XP_006723795.1:p.His83Leu
XM_011528647.1:c.542A>T XP_011526949.1:p.His181Leu
XM_011528648.1:c.539A>T XP_011526950.1:p.His180Leu
XM_011528649.1:c.458A>T XP_011526951.1:p.His153Leu
XM_011528650.1:c.542A>T XP_011526952.1:p.His181Leu
XM_011528651.1:c.257A>T XP_011526953.1:p.His86Leu
XM_011528652.1:c.194A>T XP_011526954.1:p.His65Leu
NM_001363734.1:c.248A>T NP_001350663.1:p.His83Leu
XM_006723727.3:c.275A>T XP_006723790.1:p.His92Leu
XM_006723728.3:c.248A>T XP_006723791.1:p.His83Leu
XM_006723730.4:c.194A>T XP_006723793.1:p.His65Leu
XM_011528648.3:c.539A>T XP_011526950.1:p.His180Leu
XM_011528652.2:c.194A>T XP_011526954.1:p.His65Leu
XM_017027704.1:c.194A>T XP_016883193.1:p.His65Leu
XM_017027705.1:c.194A>T XP_016883194.1:p.His65Leu
XM_017027706.1:c.278A>T XP_016883195.1:p.His93Leu
NM_015338.6:c.278A>T MANE Select NP_056153.2:p.His93Leu