Canonical Allele Identifier: CA2510575807
Gene: IFNL3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.39244283del , CM000681.2:g.39244283del GRCh38
NC_000019.9:g.39734923del , CM000681.1:g.39734923del GRCh37
NC_000019.8:g.44426763del NCBI36
NG_042193.1:g.5689del

Transcript Alleles

HGVS Amino-acid Change
ENST00000613087.5:c.271-126del ENSP00000481633.1:n.271-126del
ENST00000413851.3:c.259-126del MANE Select ENSP00000409000.2:n.259-126del
ENST00000413851.2:c.259-126del ENSP00000409000.2:n.259-126del
ENST00000613087.4:c.271-126del ENSP00000481633.1:n.271-126del
NM_172139.2:c.259-126del NP_742151.2:n.259-126del
XM_005258765.3:c.271-126del XP_005258822.1:n.271-126del
XM_011526757.1:c.271-126del XP_011525059.1:n.271-126del
NM_001346937.1:c.271-126del NP_001333866.1:n.271-126del
NM_172139.3:c.259-126del NP_742151.2:n.259-126del
NM_172139.4:c.259-126del MANE Select NP_742151.2:n.259-126del
NM_001346937.2:c.271-126del NP_001333866.1:n.271-126del