Canonical Allele Identifier: CA2522527033

Gene: IFNL3

Linked Data

• gnomAD v4: 19-39244308-TGTGGGGAGAGGAGAGAGGGACAATGGAGAAGGAGAAGGTGAAGGGGCCACTACAGAGCCAG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.39244312_39244372del , CM000681.2:g.39244312_39244372del	GRCh38
NC_000019.9:g.39734952_39735012del , CM000681.1:g.39734952_39735012del	GRCh37
NC_000019.8:g.44426792_44426852del	NCBI36
NG_042193.1:g.5603_5663del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000613087.5:c.270+48_270+108del	ENSP00000481633.1:n.270+48_270+108del
ENST00000413851.3:c.258+48_258+108del MANE Select	ENSP00000409000.2:n.258+48_258+108del
ENST00000413851.2:c.258+48_258+108del	ENSP00000409000.2:n.258+48_258+108del
ENST00000613087.4:c.270+48_270+108del	ENSP00000481633.1:n.270+48_270+108del
NM_172139.2:c.258+48_258+108del	NP_742151.2:n.258+48_258+108del
XM_005258765.3:c.270+48_270+108del	XP_005258822.1:n.270+48_270+108del
XM_011526757.1:c.270+48_270+108del	XP_011525059.1:n.270+48_270+108del
NM_001346937.1:c.270+48_270+108del	NP_001333866.1:n.270+48_270+108del
NM_172139.3:c.258+48_258+108del	NP_742151.2:n.258+48_258+108del
NM_172139.4:c.258+48_258+108del MANE Select	NP_742151.2:n.258+48_258+108del
NM_001346937.2:c.270+48_270+108del	NP_001333866.1:n.270+48_270+108del