Canonical Allele Identifier: CA617991676
Gene: TNFAIP8L3 HGNC NCBI
PIRC66 HGNC NCBI
MIR4713HG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.51060052A>T , CM000677.2:g.51060052A>T GRCh38
NC_000015.9:g.51352249A>T , CM000677.1:g.51352249A>T GRCh37
NC_000015.8:g.49139541A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000637513.2:c.53-1609T>A (TNFAIP8L3) MANE Select ENSP00000489743.1:n.53-1609T>A
ENST00000649177.1:c.-86-1609T>A (TNFAIP8L3) ENSP00000498365.1:n.-86-1609T>A
ENST00000327536.5:c.317-1609T>A (TNFAIP8L3) ENSP00000328016.5:n.317-1609T>A
NM_001311175.1:c.53-1609T>A (TNFAIP8L3) NP_001298104.1:n.53-1609T>A
NM_207381.3:c.317-1609T>A (TNFAIP8L3) NP_997264.2:n.317-1609T>A
XM_006720500.2:c.-86-1609T>A (TNFAIP8L3) XP_006720563.1:n.-86-1609T>A
XM_011521545.1:c.95-1609T>A (TNFAIP8L3) XP_011519847.1:n.95-1609T>A
XM_011521546.1:c.50-1609T>A (TNFAIP8L3) XP_011519848.1:n.50-1609T>A
XR_932222.1:n.98+22371A>T (PIRC66)
NR_146310.1:n.194+22371A>T (MIR4713HG)
XM_011521545.2:c.95-1609T>A (TNFAIP8L3) XP_011519847.1:n.95-1609T>A
XM_017022168.1:c.50-1609T>A (TNFAIP8L3) XP_016877657.1:n.50-1609T>A
XM_017022169.1:c.-86-1609T>A (TNFAIP8L3) XP_016877658.1:n.-86-1609T>A
NM_001311175.2:c.53-1609T>A (TNFAIP8L3) MANE Select NP_001298104.1:n.53-1609T>A
NM_207381.4:c.317-1609T>A (TNFAIP8L3) NP_997264.2:n.317-1609T>A