Canonical Allele Identifier: CA2612150416

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5249390_5249393dup , CM000673.2:g.5249390_5249393dup GRCh38
NC_000011.9:g.5270620_5270623dup , CM000673.1:g.5270620_5270623dup GRCh37
NC_000011.8:g.5227196_5227199dup NCBI36
NG_000007.3:g.48225_48228dup

Transcript Alleles

HGVS Amino-acid change
ENST00000330597.5:c.292_295dup (HBG1) MANE Select ENSP00000327431.4:p.Val99AlafsTer5
ENST00000642908.1:c.316-904_316-901dup ENSP00000495346.1:n.316-904_316-901dup
ENST00000647543.1:c.379-904_379-901dup ENSP00000496470.1:n.379-904_379-901dup
ENST00000648735.1:n.343_346dup (HBG1)
ENST00000330597.3:c.292_295dup (HBG1) ENSP00000327431.3:p.Val99AlafsTer5
ENST00000620888.4:c.316-904_316-901dup (HBG2) ENSP00000479637.1:n.316-904_316-901dup
ENST00000623781.1:c.62_65dup ENSP00000485381.1:p.Gln22HisfsTer17
ENST00000632727.1:c.*161_*164dup (HBG1) ENSP00000488759.1:n.*161_*164dup
NM_000559.2:c.292_295dup (HBG1) NP_000550.2:p.Val99AlafsTer5
NM_000559.3:c.292_295dup (HBG1) MANE Select NP_000550.2:p.Val99AlafsTer5