Canonical Allele Identifier: CA2200882856
Gene: HBA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.176784_176785delinsGC , CM000678.2:g.176784_176785delinsGC GRCh38
NC_000016.9:g.226783_226784delinsGC , CM000678.1:g.226783_226784delinsGC GRCh37
NC_000016.8:g.166783_166784delinsGC NCBI36
NG_000006.1:g.37647_37648delinsGC
NG_059186.1:g.5134_5135delinsGC

Transcript Alleles

HGVS Amino-acid change
ENST00000320868.9:c.68_69delinsGC MANE Select ENSP00000322421.5:p.Gly23=
ENST00000397797.1:c.-2+22_-2+23delinsGC ENSP00000380899.1:n.-2+22_-2+23delinsGC
ENST00000472694.1:n.87_88delinsGC
ENST00000487791.1:n.37_38delinsGC
NM_000558.4:c.68_69delinsGC NP_000549.1:p.Gly23=
NM_000558.5:c.68_69delinsGC MANE Select NP_000549.1:p.Gly23=