Canonical Allele Identifier: CA432228073

Gene: TRAF3IP1

Linked Data

• MyVariant Identifiers: chr2:g.239306108T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.238397467T>C , CM000664.2:g.238397467T>C	GRCh38
NC_000002.11:g.239306108T>C , CM000664.1:g.239306108T>C	GRCh37
NC_000002.10:g.238970847T>C	NCBI36
NG_053055.1:g.81979T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373327.5:c.1698T>C MANE Select	ENSP00000362424.4:p.Ser566=
ENST00000373327.4:c.1698T>C	ENSP00000362424.4:p.Ser566=
ENST00000391993.7:c.1500T>C	ENSP00000375851.3:p.Ser500=
ENST00000462122.1:n.709T>C
ENST00000483951.1:n.46T>C
NM_001139490.1:c.1500T>C	NP_001132962.1:p.Ser500=
NM_015650.3:c.1698T>C	NP_056465.2:p.Ser566=
XM_006712414.1:c.1497T>C	XP_006712477.1:p.Ser499=
XM_011510944.1:c.1800T>C	XP_011509246.1:p.Ser600=
XM_011510945.1:c.1761T>C	XP_011509247.1:p.Ser587=
XM_011510946.1:c.1728T>C	XP_011509248.1:p.Ser576=
XM_011510947.1:c.1668T>C	XP_011509249.1:p.Ser556=
XM_011510948.1:c.1602T>C	XP_011509250.1:p.Ser534=
XM_011510950.1:c.666T>C	XP_011509252.1:p.Ser222=
XR_922902.1:n.1997T>C
XM_006712414.2:c.1497T>C	XP_006712477.1:p.Ser499=
XM_011510944.2:c.1800T>C	XP_011509246.1:p.Ser600=
XM_011510945.2:c.1761T>C	XP_011509247.1:p.Ser587=
XM_011510946.2:c.1728T>C	XP_011509248.1:p.Ser576=
XM_011510947.2:c.1668T>C	XP_011509249.1:p.Ser556=
XM_011510948.2:c.1602T>C	XP_011509250.1:p.Ser534=
XM_011510950.2:c.666T>C	XP_011509252.1:p.Ser222=
XM_017003789.1:c.1797T>C	XP_016859278.1:p.Ser599=
XR_001738696.1:n.1526T>C
XR_001738697.1:n.1523T>C
XR_922902.2:n.2060T>C
NM_015650.4:c.1698T>C MANE Select	NP_056465.2:p.Ser566=