Canonical Allele Identifier: CA2335422137

Gene: IFNL3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.39244583_39244584delinsAG , CM000681.2:g.39244583_39244584delinsAG	GRCh38
NC_000019.9:g.39735223_39735224delinsAG , CM000681.1:g.39735223_39735224delinsAG	GRCh37
NC_000019.8:g.44427063_44427064delinsAG	NCBI36
NG_042193.1:g.5388_5389delinsCT
NG_055295.1:g.9273_9274delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000613087.5:c.193-90_193-89delinsCT	ENSP00000481633.1:n.193-90_193-89delinsCT
ENST00000413851.3:c.181-90_181-89delinsCT MANE Select	ENSP00000409000.2:n.181-90_181-89delinsCT
ENST00000413851.2:c.181-90_181-89delinsCT	ENSP00000409000.2:n.181-90_181-89delinsCT
ENST00000613087.4:c.193-90_193-89delinsCT	ENSP00000481633.1:n.193-90_193-89delinsCT
NM_172139.2:c.181-90_181-89delinsCT	NP_742151.2:n.181-90_181-89delinsCT
XM_005258765.3:c.193-90_193-89delinsCT	XP_005258822.1:n.193-90_193-89delinsCT
XM_011526757.1:c.193-90_193-89delinsCT	XP_011525059.1:n.193-90_193-89delinsCT
NM_001346937.1:c.193-90_193-89delinsCT	NP_001333866.1:n.193-90_193-89delinsCT
NM_172139.3:c.181-90_181-89delinsCT	NP_742151.2:n.181-90_181-89delinsCT
NM_172139.4:c.181-90_181-89delinsCT MANE Select	NP_742151.2:n.181-90_181-89delinsCT
NM_001346937.2:c.193-90_193-89delinsCT	NP_001333866.1:n.193-90_193-89delinsCT