Canonical Allele Identifier: CA2574735791

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5249397del , CM000673.2:g.5249397del GRCh38
NC_000011.9:g.5270627del , CM000673.1:g.5270627del GRCh37
NC_000011.8:g.5227203del NCBI36
NG_000007.3:g.48220del

Transcript Alleles

HGVS Amino-acid change
ENST00000330597.5:c.287del (HBG1) MANE Select ENSP00000327431.4:p.Lys96SerfsTer17
ENST00000642908.1:c.316-909del ENSP00000495346.1:n.316-909del
ENST00000647543.1:c.379-909del ENSP00000496470.1:n.379-909del
ENST00000648735.1:n.338del (HBG1)
ENST00000330597.3:c.287del (HBG1) ENSP00000327431.3:p.Lys96SerfsTer17
ENST00000620888.4:c.316-909del (HBG2) ENSP00000479637.1:n.316-909del
ENST00000623781.1:c.69del ENSP00000485381.1:p.Val24SerfsTer?
ENST00000632727.1:c.*156del (HBG1) ENSP00000488759.1:n.*156del
NM_000559.2:c.287del (HBG1) NP_000550.2:p.Lys96SerfsTer17
NM_000559.3:c.287del (HBG1) MANE Select NP_000550.2:p.Lys96SerfsTer17