Canonical Allele Identifier: CA2695221230
Gene: HBA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.176954_176959del , CM000678.2:g.176954_176959del GRCh38
NC_000016.9:g.226953_226958del , CM000678.1:g.226953_226958del GRCh37
NC_000016.8:g.166953_166958del NCBI36
NG_000006.1:g.37817_37822del
NG_059186.1:g.5304_5309del

Transcript Alleles

HGVS Amino-acid change
ENST00000320868.9:c.121_126del MANE Select ENSP00000322421.5:p.Lys41_Thr42del
ENST00000397797.1:c.25_30del ENSP00000380899.1:p.Lys9_Thr10del
ENST00000472694.1:n.257_262del
ENST00000487791.1:n.90_95del
NM_000558.4:c.121_126del NP_000549.1:p.Lys41_Thr42del
NM_000558.5:c.121_126del MANE Select NP_000549.1:p.Lys41_Thr42del