Canonical Allele Identifier: CA2200880883

Gene: HBA2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.173461_173466delinsTCTCTG , CM000678.2:g.173461_173466delinsTCTCTG	GRCh38
NC_000016.9:g.223460_223465delinsTCTCTG , CM000678.1:g.223460_223465delinsTCTCTG	GRCh37
NC_000016.8:g.163460_163465delinsTCTCTG	NCBI36
NG_000006.1:g.34324_34329delinsTCTCTG
NG_059186.1:g.1811_1816delinsTCTCTG
NG_059271.1:g.5615_5620delinsTCTCTG

Transcript Alleles

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