Canonical Allele Identifier: CA2176711090

Gene: TNFAIP8L3 PIRC66 MIR4713HG

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.51083537C= , CM000677.2:g.51083537C=	GRCh38
NC_000015.9:g.51375734C= , CM000677.1:g.51375734C=	GRCh37
NC_000015.8:g.49163026C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000637513.2:c.52+11007G= (TNFAIP8L3) MANE Select	ENSP00000489743.1:n.52+11007G=
ENST00000649177.1:c.-87+10874G= (TNFAIP8L3)	ENSP00000498365.1:n.-87+10874G=
ENST00000327536.5:c.316+11007G= (TNFAIP8L3)	ENSP00000328016.5:n.316+11007G=
NM_001311175.1:c.52+11007G= (TNFAIP8L3)	NP_001298104.1:n.52+11007G=
NM_207381.3:c.316+11007G= (TNFAIP8L3)	NP_997264.2:n.316+11007G=
XM_006720500.2:c.-87+1510G= (TNFAIP8L3)	XP_006720563.1:n.-87+1510G=
XR_932222.1:n.98+45856C= (PIRC66)
NR_146310.1:n.194+45856C= (MIR4713HG)
XM_017022169.1:c.-87+1510G= (TNFAIP8L3)	XP_016877658.1:n.-87+1510G=
NM_001311175.2:c.52+11007G= (TNFAIP8L3) MANE Select	NP_001298104.1:n.52+11007G=
NM_207381.4:c.316+11007G= (TNFAIP8L3)	NP_997264.2:n.316+11007G=