Canonical Allele Identifier: CA2335422006

Gene: IFNL3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.39244375_39244376delinsCA , CM000681.2:g.39244375_39244376delinsCA	GRCh38
NC_000019.9:g.39735015_39735016delinsCA , CM000681.1:g.39735015_39735016delinsCA	GRCh37
NC_000019.8:g.44426855_44426856delinsCA	NCBI36
NG_042193.1:g.5596_5597delinsTG
NG_055295.1:g.9481_9482delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000613087.5:c.270+41_270+42delinsTG	ENSP00000481633.1:n.270+41_270+42delinsTG
ENST00000413851.3:c.258+41_258+42delinsTG MANE Select	ENSP00000409000.2:n.258+41_258+42delinsTG
ENST00000413851.2:c.258+41_258+42delinsTG	ENSP00000409000.2:n.258+41_258+42delinsTG
ENST00000613087.4:c.270+41_270+42delinsTG	ENSP00000481633.1:n.270+41_270+42delinsTG
NM_172139.2:c.258+41_258+42delinsTG	NP_742151.2:n.258+41_258+42delinsTG
XM_005258765.3:c.270+41_270+42delinsTG	XP_005258822.1:n.270+41_270+42delinsTG
XM_011526757.1:c.270+41_270+42delinsTG	XP_011525059.1:n.270+41_270+42delinsTG
NM_001346937.1:c.270+41_270+42delinsTG	NP_001333866.1:n.270+41_270+42delinsTG
NM_172139.3:c.258+41_258+42delinsTG	NP_742151.2:n.258+41_258+42delinsTG
NM_172139.4:c.258+41_258+42delinsTG MANE Select	NP_742151.2:n.258+41_258+42delinsTG
NM_001346937.2:c.270+41_270+42delinsTG	NP_001333866.1:n.270+41_270+42delinsTG