Canonical Allele Identifier: CA5350387

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136925969G>T , CM000671.2:g.136925969G>T GRCh38
NC_000009.11:g.139820421G>T , CM000671.1:g.139820421G>T GRCh37
NC_000009.10:g.138940242G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000247668.7:c.*68G>T (TRAF2) MANE Select ENSP00000247668.2:n.*68G>T
ENST00000247668.6:c.*68G>T (TRAF2) ENSP00000247668.2:n.*68G>T
ENST00000432842.6:c.*1038-31750G>T (RABL6) ENSP00000414081.3:n.*1038-31750G>T
NM_021138.3:c.*68G>T (TRAF2) NP_066961.2:n.*68G>T
XM_005266099.3:c.*68G>T (TRAF2) XP_005266156.1:n.*68G>T
XM_011518973.1:c.*68G>T (TRAF2) XP_011517275.1:n.*68G>T
XM_011518974.1:c.*68G>T (TRAF2) XP_011517276.1:n.*68G>T
XM_011518975.1:c.*68G>T (TRAF2) XP_011517277.1:n.*68G>T
XM_011518976.1:c.*68G>T (TRAF2) XP_011517278.1:n.*68G>T
XM_011518977.1:c.*68G>T (TRAF2) XP_011517279.1:n.*68G>T
XM_011518978.1:c.*68G>T (TRAF2) XP_011517280.1:n.*68G>T
XM_011518974.2:c.*68G>T (TRAF2) XP_011517276.1:n.*68G>T
XM_011518976.3:c.*68G>T (TRAF2) XP_011517278.1:n.*68G>T
XM_011518977.2:c.*68G>T (TRAF2) XP_011517279.1:n.*68G>T
NM_021138.4:c.*68G>T (TRAF2) MANE Select NP_066961.2:n.*68G>T