Canonical Allele Identifier: CA2200880229

Gene: HBA2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.172929_172932delinsCCGA , CM000678.2:g.172929_172932delinsCCGA	GRCh38
NC_000016.9:g.222928_222931delinsCCGA , CM000678.1:g.222928_222931delinsCCGA	GRCh37
NC_000016.8:g.162928_162931delinsCCGA	NCBI36
NG_000006.1:g.33792_33795delinsCCGA
NG_059186.1:g.1279_1282delinsCCGA
NG_059271.1:g.5083_5086delinsCCGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251595.11:c.17_20delinsCCGA MANE Select	ENSP00000251595.6:p.Ala6=
ENST00000251595.10:c.17_20delinsCCGA	ENSP00000251595.6:p.Ala6=
ENST00000397806.1:c.-31_-28delinsCCGA	ENSP00000380908.1:n.-31_-28delinsCCGA
ENST00000482565.1:n.36_39delinsCCGA
NM_000517.4:c.17_20delinsCCGA	NP_000508.1:p.Ala6=
NM_000517.6:c.17_20delinsCCGA MANE Select	NP_000508.1:p.Ala6=