Canonical Allele Identifier: CA267153210

Gene: TNFAIP2

Linked Data

• dbSNP Id: rs34735806
• MyVariant Identifiers: chr14:g.103603568del (hg19) ; chr14:g.103137231del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.103137232del , CM000676.2:g.103137232del	GRCh38
NC_000014.8:g.103603569del , CM000676.1:g.103603569del	GRCh37
NC_000014.7:g.102673322del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000333007.8:c.*1872del	ENSP00000332326.1:n.*1872del
ENST00000560869.6:c.*1872del MANE Select	ENSP00000452634.2:n.*1872del
ENST00000333007.5:c.*1872del	ENSP00000332326.1:n.*1872del
ENST00000560869.5:c.*1872del	ENSP00000452634.1:n.*1872del
ENST00000561217.1:n.403del
NM_006291.2:c.*1872del	NP_006282.2:n.*1872del
XM_006720243.2:c.*1229del	XP_006720306.1:n.*1229del
XM_011537112.1:c.*1229del	XP_011535414.1:n.*1229del
XM_011537113.1:c.*1229del	XP_011535415.1:n.*1229del
XM_011537114.1:c.*1872del	XP_011535416.1:n.*1872del
XM_006720243.3:c.*1229del	XP_006720306.1:n.*1229del
XM_011537112.2:c.*1229del	XP_011535414.1:n.*1229del
XM_011537113.2:c.*1229del	XP_011535415.1:n.*1229del
XM_011537114.2:c.*1872del	XP_011535416.1:n.*1872del
XM_017021616.1:c.*1229del	XP_016877105.1:n.*1229del
NM_006291.3:c.*1872del	NP_006282.2:n.*1872del
NM_001371220.1:c.*1229del	NP_001358149.1:n.*1229del
NM_001371221.1:c.*1229del	NP_001358150.1:n.*1229del
NM_006291.4:c.*1872del MANE Select	NP_006282.2:n.*1872del