Canonical Allele Identifier: CA3268250546
Community Standard Title: NM_000558.5(HBA1):c.43_45delinsCGA (p.Trp15Arg)
Gene: HBA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.176759_176761delinsCGA , CM000678.2:g.176759_176761delinsCGA GRCh38
NC_000016.9:g.226758_226760delinsCGA , CM000678.1:g.226758_226760delinsCGA GRCh37
NC_000016.8:g.166758_166760delinsCGA NCBI36
NG_000006.1:g.37622_37624delinsCGA
NG_059186.1:g.5109_5111delinsCGA

Transcript Alleles

HGVS Amino-acid Change
NM_000558.5:c.43_45delinsCGA MANE Select NP_000549.1:p.Trp15Arg
ENST00000320868.9:c.43_45delinsCGA MANE Select ENSP00000322421.5:p.Trp15Arg
NM_000558.4:c.43_45delinsCGA NP_000549.1:p.Trp15Arg
ENST00000397797.1:c.-5_-3delinsCGA ENSP00000380899.1:n.-5_-3delinsCGA
ENST00000472694.1:n.62_64delinsCGA
ENST00000487791.1:n.12_14delinsCGA