Canonical Allele Identifier: CA162411

Gene: TNFAIP3

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.137874923C>T , CM000668.2:g.137874923C>T	GRCh38
NC_000006.11:g.138196060C>T , CM000668.1:g.138196060C>T	GRCh37
NC_000006.10:g.138237753C>T	NCBI36
NG_032761.1:g.12480C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000420009.6:c.374C>T	ENSP00000401562.2:p.Ala125Val
ENST00000711061.1:c.*97C>T	ENSP00000518561.1:n.*97C>T
ENST00000421450.2:c.374C>T	ENSP00000393577.2:p.Ala125Val
ENST00000433680.2:c.374C>T	ENSP00000409845.2:p.Ala125Val
ENST00000485192.2:n.183C>T
ENST00000698329.1:n.563C>T
ENST00000698330.1:n.295+3401C>T
ENST00000612899.5:c.374C>T MANE Select	ENSP00000481570.1:p.Ala125Val
ENST00000237289.8:c.374C>T	ENSP00000237289.4:p.Ala125Val
ENST00000420009.5:c.374C>T	ENSP00000401562.1:p.Ala125Val
ENST00000612899.4:c.374C>T	ENSP00000481570.1:p.Ala125Val
ENST00000614035.4:c.374C>T	ENSP00000481122.2:p.Ala125Val
ENST00000615468.4:c.374C>T	ENSP00000479556.1:p.Ala125Val
ENST00000619035.4:c.374C>T	ENSP00000478438.1:p.Ala125Val
ENST00000620204.3:c.374C>T	ENSP00000481454.1:p.Ala125Val
ENST00000621150.3:c.374C>T	ENSP00000484332.2:p.Ala125Val
NM_001270507.1:c.374C>T	NP_001257436.1:p.Ala125Val
NM_001270508.1:c.374C>T	NP_001257437.1:p.Ala125Val
NM_006290.3:c.374C>T	NP_006281.1:p.Ala125Val
XM_005267119.1:c.374C>T	XP_005267176.1:p.Ala125Val
XM_006715555.1:c.-278C>T	XP_006715618.1:n.-278C>T
XM_011536095.1:c.374C>T	XP_011534397.1:p.Ala125Val
XM_011536096.1:c.374C>T	XP_011534398.1:p.Ala125Val
XM_011536096.2:c.374C>T	XP_011534398.1:p.Ala125Val
XM_024446532.1:c.374C>T	XP_024302300.1:p.Ala125Val
XM_024446533.1:c.374C>T	XP_024302301.1:p.Ala125Val
NM_001270508.2:c.374C>T MANE Select	NP_001257437.1:p.Ala125Val
NM_001270507.2:c.374C>T	NP_001257436.1:p.Ala125Val
NM_006290.4:c.374C>T	NP_006281.1:p.Ala125Val