Canonical Allele Identifier: CA2200880922
Gene: HBA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.173514_173517delinsCCCG , CM000678.2:g.173514_173517delinsCCCG GRCh38
NC_000016.9:g.223513_223516delinsCCCG , CM000678.1:g.223513_223516delinsCCCG GRCh37
NC_000016.8:g.163513_163516delinsCCCG NCBI36
NG_000006.1:g.34377_34380delinsCCCG
NG_059186.1:g.1864_1867delinsCCCG
NG_059271.1:g.5668_5671delinsCCCG

Transcript Alleles

HGVS Amino-acid change
ENST00000251595.11:c.343_346delinsCCCG MANE Select ENSP00000251595.6:p.Pro115=
ENST00000251595.10:c.343_346delinsCCCG ENSP00000251595.6:p.Pro115=
ENST00000397806.1:c.247_250delinsCCCG ENSP00000380908.1:p.Pro83=
ENST00000482565.1:n.479_482delinsCCCG
NM_000517.4:c.343_346delinsCCCG NP_000508.1:p.Pro115=
NM_000517.6:c.343_346delinsCCCG MANE Select NP_000508.1:p.Pro115=