Canonical Allele Identifier: CA2200882835
Gene: HBA1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.176759_176760delinsTG , CM000678.2:g.176759_176760delinsTG GRCh38
NC_000016.9:g.226758_226759delinsTG , CM000678.1:g.226758_226759delinsTG GRCh37
NC_000016.8:g.166758_166759delinsTG NCBI36
NG_000006.1:g.37622_37623delinsTG
NG_059186.1:g.5109_5110delinsTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000320868.9:c.43_44delinsTG MANE Select ENSP00000322421.5:p.Trp15=
ENST00000397797.1:c.-5_-4delinsTG ENSP00000380899.1:n.-5_-4delinsTG
ENST00000472694.1:n.62_63delinsTG
ENST00000487791.1:n.12_13delinsTG
NM_000558.4:c.43_44delinsTG NP_000549.1:p.Trp15=
NM_000558.5:c.43_44delinsTG MANE Select NP_000549.1:p.Trp15=
Search 100 bp 5'
Search 100 bp 3'