Canonical Allele Identifier: CA2200880869

Gene: HBA2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.173443_173452delinsGGGCCGCACT , CM000678.2:g.173443_173452delinsGGGCCGCACT	GRCh38
NC_000016.9:g.223442_223451delinsGGGCCGCACT , CM000678.1:g.223442_223451delinsGGGCCGCACT	GRCh37
NC_000016.8:g.163442_163451delinsGGGCCGCACT	NCBI36
NG_000006.1:g.34306_34315delinsGGGCCGCACT
NG_059186.1:g.1793_1802delinsGGGCCGCACT
NG_059271.1:g.5597_5606delinsGGGCCGCACT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251595.11:c.301-29_301-20delinsGGGCCGCACT MANE Select	ENSP00000251595.6:n.301-29_301-20delinsGGGCCGCACT
ENST00000251595.10:c.301-29_301-20delinsGGGCCGCACT	ENSP00000251595.6:n.301-29_301-20delinsGGGCCGCACT
ENST00000397806.1:c.205-29_205-20delinsGGGCCGCACT	ENSP00000380908.1:n.205-29_205-20delinsGGGCCGCACT
ENST00000482565.1:n.437-29_437-20delinsGGGCCGCACT
ENST00000484216.1:n.383_392delinsGGGCCGCACT
NM_000517.4:c.301-29_301-20delinsGGGCCGCACT	NP_000508.1:n.301-29_301-20delinsGGGCCGCACT
NM_000517.6:c.301-29_301-20delinsGGGCCGCACT MANE Select	NP_000508.1:n.301-29_301-20delinsGGGCCGCACT