Canonical Allele Identifier: CA713599035

Gene: TNFAIP8L3 PIRC66 MIR4713HG

Linked Data

• dbSNP Id: rs3803369
• MyVariant Identifiers: chr15:g.51375829T>A (hg19) ; chr15:g.51083632T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.51083632T>A , CM000677.2:g.51083632T>A	GRCh38
NC_000015.9:g.51375829T>A , CM000677.1:g.51375829T>A	GRCh37
NC_000015.8:g.49163121T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000637513.2:c.52+10912A>T (TNFAIP8L3) MANE Select	ENSP00000489743.1:n.52+10912A>T
ENST00000649177.1:c.-87+10779A>T (TNFAIP8L3)	ENSP00000498365.1:n.-87+10779A>T
ENST00000327536.5:c.316+10912A>T (TNFAIP8L3)	ENSP00000328016.5:n.316+10912A>T
NM_001311175.1:c.52+10912A>T (TNFAIP8L3)	NP_001298104.1:n.52+10912A>T
NM_207381.3:c.316+10912A>T (TNFAIP8L3)	NP_997264.2:n.316+10912A>T
XM_006720500.2:c.-87+1415A>T (TNFAIP8L3)	XP_006720563.1:n.-87+1415A>T
XR_932222.1:n.98+45951T>A (PIRC66)
NR_146310.1:n.194+45951T>A (MIR4713HG)
XM_017022169.1:c.-87+1415A>T (TNFAIP8L3)	XP_016877658.1:n.-87+1415A>T
NM_001311175.2:c.52+10912A>T (TNFAIP8L3) MANE Select	NP_001298104.1:n.52+10912A>T
NM_207381.4:c.316+10912A>T (TNFAIP8L3)	NP_997264.2:n.316+10912A>T