Canonical Allele Identifier: CA2198063
Community Standard Title: NM_015650.4(TRAF3IP1):c.436T>C (p.Ser146Pro)
Gene: TRAF3IP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.238328767T>C , CM000664.2:g.238328767T>C GRCh38
NC_000002.11:g.239237408T>C , CM000664.1:g.239237408T>C GRCh37
NC_000002.10:g.238902147T>C NCBI36
NG_053055.1:g.13279T>C

Transcript Alleles

HGVS Amino-acid Change
NM_015650.4:c.436T>C MANE Select NP_056465.2:p.Ser146Pro
ENST00000373327.5:c.436T>C MANE Select ENSP00000362424.4:p.Ser146Pro
NM_001139490.1:c.436T>C NP_001132962.1:p.Ser146Pro
NM_015650.3:c.436T>C NP_056465.2:p.Ser146Pro
ENST00000373327.4:c.436T>C ENSP00000362424.4:p.Ser146Pro
ENST00000391993.7:c.436T>C ENSP00000375851.3:p.Ser146Pro
ENST00000409739.2:c.*305T>C ENSP00000386648.2:n.*305T>C
XM_006712414.1:c.436T>C XP_006712477.1:p.Ser146Pro
XM_006712414.2:c.436T>C XP_006712477.1:p.Ser146Pro
XM_011510944.1:c.436T>C XP_011509246.1:p.Ser146Pro
XM_011510944.2:c.436T>C XP_011509246.1:p.Ser146Pro
XM_011510945.1:c.436T>C XP_011509247.1:p.Ser146Pro
XM_011510945.2:c.436T>C XP_011509247.1:p.Ser146Pro
XM_011510946.1:c.436T>C XP_011509248.1:p.Ser146Pro
XM_011510946.2:c.436T>C XP_011509248.1:p.Ser146Pro
XM_011510947.1:c.304T>C XP_011509249.1:p.Ser102Pro
XM_011510947.2:c.304T>C XP_011509249.1:p.Ser102Pro
XM_011510948.1:c.436T>C XP_011509250.1:p.Ser146Pro
XM_011510948.2:c.436T>C XP_011509250.1:p.Ser146Pro
XM_011510949.1:c.436T>C XP_011509251.1:p.Ser146Pro
XM_017003789.1:c.436T>C XP_016859278.1:p.Ser146Pro
XR_001738696.1:n.610T>C
XR_001738697.1:n.610T>C
XR_922902.1:n.547T>C
XR_922902.2:n.610T>C