Canonical Allele Identifier: CA1338105435
Gene: TRAF3IP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.238397509C= , CM000664.2:g.238397509C= GRCh38
NC_000002.11:g.239306150C= , CM000664.1:g.239306150C= GRCh37
NC_000002.10:g.238970889C= NCBI36
NG_053055.1:g.82021C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000373327.5:c.1740C= MANE Select ENSP00000362424.4:p.Ser580=
ENST00000373327.4:c.1740C= ENSP00000362424.4:p.Ser580=
ENST00000391993.7:c.1542C= ENSP00000375851.3:p.Ser514=
ENST00000462122.1:n.751C=
ENST00000483951.1:n.88C=
NM_001139490.1:c.1542C= NP_001132962.1:p.Ser514=
NM_015650.3:c.1740C= NP_056465.2:p.Ser580=
XM_006712414.1:c.1539C= XP_006712477.1:p.Ser513=
XM_011510944.1:c.1842C= XP_011509246.1:p.Ser614=
XM_011510945.1:c.1803C= XP_011509247.1:p.Ser601=
XM_011510946.1:c.1770C= XP_011509248.1:p.Ser590=
XM_011510947.1:c.1710C= XP_011509249.1:p.Ser570=
XM_011510948.1:c.1644C= XP_011509250.1:p.Ser548=
XM_011510950.1:c.708C= XP_011509252.1:p.Ser236=
XR_922902.1:n.2039C=
XM_006712414.2:c.1539C= XP_006712477.1:p.Ser513=
XM_011510944.2:c.1842C= XP_011509246.1:p.Ser614=
XM_011510945.2:c.1803C= XP_011509247.1:p.Ser601=
XM_011510946.2:c.1770C= XP_011509248.1:p.Ser590=
XM_011510947.2:c.1710C= XP_011509249.1:p.Ser570=
XM_011510948.2:c.1644C= XP_011509250.1:p.Ser548=
XM_011510950.2:c.708C= XP_011509252.1:p.Ser236=
XM_017003789.1:c.1839C= XP_016859278.1:p.Ser613=
XR_001738696.1:n.1568C=
XR_001738697.1:n.1565C=
XR_922902.2:n.2102C=
NM_015650.4:c.1740C= MANE Select NP_056465.2:p.Ser580=