Canonical Allele Identifier: CA2335422096

Gene: IFNL3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.39244514_39244515delinsGT , CM000681.2:g.39244514_39244515delinsGT	GRCh38
NC_000019.9:g.39735154_39735155delinsGT , CM000681.1:g.39735154_39735155delinsGT	GRCh37
NC_000019.8:g.44426994_44426995delinsGT	NCBI36
NG_042193.1:g.5457_5458delinsAC
NG_055295.1:g.9342_9343delinsAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000613087.5:c.193-21_193-20delinsAC	ENSP00000481633.1:n.193-21_193-20delinsAC
ENST00000413851.3:c.181-21_181-20delinsAC MANE Select	ENSP00000409000.2:n.181-21_181-20delinsAC
ENST00000413851.2:c.181-21_181-20delinsAC	ENSP00000409000.2:n.181-21_181-20delinsAC
ENST00000613087.4:c.193-21_193-20delinsAC	ENSP00000481633.1:n.193-21_193-20delinsAC
NM_172139.2:c.181-21_181-20delinsAC	NP_742151.2:n.181-21_181-20delinsAC
XM_005258765.3:c.193-21_193-20delinsAC	XP_005258822.1:n.193-21_193-20delinsAC
XM_011526757.1:c.193-21_193-20delinsAC	XP_011525059.1:n.193-21_193-20delinsAC
NM_001346937.1:c.193-21_193-20delinsAC	NP_001333866.1:n.193-21_193-20delinsAC
NM_172139.3:c.181-21_181-20delinsAC	NP_742151.2:n.181-21_181-20delinsAC
NM_172139.4:c.181-21_181-20delinsAC MANE Select	NP_742151.2:n.181-21_181-20delinsAC
NM_001346937.2:c.193-21_193-20delinsAC	NP_001333866.1:n.193-21_193-20delinsAC