Canonical Allele Identifier: CA616402861

Gene: TNFAIP2

Linked Data

• dbSNP Id: rs1360098522
• gnomAD v2: 14-103603492-TC-T
• gnomAD v3: 14-103137155-TC-T
• gnomAD v4: 14-103137155-TC-T
• MyVariant Identifiers: chr14:g.103603493del (hg19) ; chr14:g.103137156del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.103137156del , CM000676.2:g.103137156del	GRCh38
NC_000014.8:g.103603493del , CM000676.1:g.103603493del	GRCh37
NC_000014.7:g.102673246del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333007.8:c.*1796del	ENSP00000332326.1:n.*1796del
ENST00000560869.6:c.*1796del MANE Select	ENSP00000452634.2:n.*1796del
ENST00000333007.5:c.*1796del	ENSP00000332326.1:n.*1796del
ENST00000560869.5:c.*1796del	ENSP00000452634.1:n.*1796del
ENST00000561217.1:n.327del
NM_006291.2:c.*1796del	NP_006282.2:n.*1796del
XM_006720243.2:c.*1153del	XP_006720306.1:n.*1153del
XM_011537112.1:c.*1153del	XP_011535414.1:n.*1153del
XM_011537113.1:c.*1153del	XP_011535415.1:n.*1153del
XM_011537114.1:c.*1796del	XP_011535416.1:n.*1796del
XM_006720243.3:c.*1153del	XP_006720306.1:n.*1153del
XM_011537112.2:c.*1153del	XP_011535414.1:n.*1153del
XM_011537113.2:c.*1153del	XP_011535415.1:n.*1153del
XM_011537114.2:c.*1796del	XP_011535416.1:n.*1796del
XM_017021616.1:c.*1153del	XP_016877105.1:n.*1153del
NM_006291.3:c.*1796del	NP_006282.2:n.*1796del
NM_001371220.1:c.*1153del	NP_001358149.1:n.*1153del
NM_001371221.1:c.*1153del	NP_001358150.1:n.*1153del
NM_006291.4:c.*1796del MANE Select	NP_006282.2:n.*1796del