Canonical Allele Identifier: CA2626702269

Gene: TNFAIP2

Linked Data

• gnomAD v4: 14-103137229-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.103137229G>T , CM000676.2:g.103137229G>T	GRCh38
NC_000014.8:g.103603566G>T , CM000676.1:g.103603566G>T	GRCh37
NC_000014.7:g.102673319G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000333007.8:c.*1869G>T	ENSP00000332326.1:n.*1869G>T
ENST00000560869.6:c.*1869G>T MANE Select	ENSP00000452634.2:n.*1869G>T
ENST00000333007.5:c.*1869G>T	ENSP00000332326.1:n.*1869G>T
ENST00000560869.5:c.*1869G>T	ENSP00000452634.1:n.*1869G>T
ENST00000561217.1:n.400G>T
NM_006291.2:c.*1869G>T	NP_006282.2:n.*1869G>T
XM_006720243.2:c.*1226G>T	XP_006720306.1:n.*1226G>T
XM_011537112.1:c.*1226G>T	XP_011535414.1:n.*1226G>T
XM_011537113.1:c.*1226G>T	XP_011535415.1:n.*1226G>T
XM_011537114.1:c.*1869G>T	XP_011535416.1:n.*1869G>T
XM_006720243.3:c.*1226G>T	XP_006720306.1:n.*1226G>T
XM_011537112.2:c.*1226G>T	XP_011535414.1:n.*1226G>T
XM_011537113.2:c.*1226G>T	XP_011535415.1:n.*1226G>T
XM_011537114.2:c.*1869G>T	XP_011535416.1:n.*1869G>T
XM_017021616.1:c.*1226G>T	XP_016877105.1:n.*1226G>T
NM_006291.3:c.*1869G>T	NP_006282.2:n.*1869G>T
NM_001371220.1:c.*1226G>T	NP_001358149.1:n.*1226G>T
NM_001371221.1:c.*1226G>T	NP_001358150.1:n.*1226G>T
NM_006291.4:c.*1869G>T MANE Select	NP_006282.2:n.*1869G>T