Canonical Allele Identifier: CA2574735792

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5249400del , CM000673.2:g.5249400del GRCh38
NC_000011.9:g.5270630del , CM000673.1:g.5270630del GRCh37
NC_000011.8:g.5227206del NCBI36
NG_000007.3:g.48216del

Transcript Alleles

HGVS Amino-acid change
ENST00000330597.5:c.283del (HBG1) MANE Select ENSP00000327431.4:p.Asp95ThrfsTer18
ENST00000642908.1:c.316-913del ENSP00000495346.1:n.316-913del
ENST00000647543.1:c.379-913del ENSP00000496470.1:n.379-913del
ENST00000648735.1:n.334del (HBG1)
ENST00000330597.3:c.283del (HBG1) ENSP00000327431.3:p.Asp95ThrfsTer18
ENST00000620888.4:c.316-913del (HBG2) ENSP00000479637.1:n.316-913del
ENST00000623781.1:c.72del ENSP00000485381.1:p.Thr25GlnfsTer?
ENST00000632727.1:c.*152del (HBG1) ENSP00000488759.1:n.*152del
NM_000559.2:c.283del (HBG1) NP_000550.2:p.Asp95ThrfsTer18
NM_000559.3:c.283del (HBG1) MANE Select NP_000550.2:p.Asp95ThrfsTer18