Canonical Allele Identifier: CA2228809
Community Standard Title: NM_182916.3(TRNT1):c.829G>T (p.Glu277Ter)

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.3147476G>T , CM000665.2:g.3147476G>T GRCh38
NC_000003.11:g.3189160G>T , CM000665.1:g.3189160G>T GRCh37
NC_000003.10:g.3164160G>T NCBI36
NG_041800.1:g.25561G>T
NG_041800.2:g.25561G>T

Transcript Alleles

HGVS Amino-acid Change
NM_182916.3:c.829G>T (TRNT1) MANE Select NP_886552.3:p.Glu277Ter
ENST00000251607.11:c.829G>T (TRNT1) MANE Select ENSP00000251607.6:p.Glu277Ter
NM_001302946.1:c.769G>T (TRNT1) NP_001289875.1:p.Glu257Ter
NM_001302946.2:c.769G>T (TRNT1) NP_001289875.2:p.Glu257Ter
NM_001367321.1:c.829G>T (TRNT1) NP_001354250.1:p.Glu277Ter
NM_001367322.1:c.829G>T (TRNT1) NP_001354251.1:p.Glu277Ter
NM_001367323.1:c.829G>T (TRNT1) NP_001354252.1:p.Glu277Ter
NM_182916.2:c.829G>T (TRNT1) NP_886552.2:p.Glu277Ter
NR_159934.1:n.907G>T (TRNT1)
NR_159935.1:n.907G>T (TRNT1)
NR_159936.1:n.713G>T (TRNT1)
NR_159937.1:n.1949G>T (TRNT1)
NR_159938.1:n.713G>T (TRNT1)
NR_159939.1:n.768G>T (TRNT1)
NR_159940.1:n.782G>T (TRNT1)
NR_159941.1:n.1949G>T (TRNT1)
ENST00000251607.10:c.829G>T (TRNT1) ENSP00000251607.6:p.Glu277Ter
ENST00000280591.10:c.769G>T (TRNT1) ENSP00000280591.6:p.Glu257Ter
ENST00000434583.5:c.829G>T (TRNT1) ENSP00000415100.1:p.Glu277Ter
ENST00000639284.1:c.1312-1977C>A (CRBN) ENSP00000491442.1:n.1312-1977C>A
ENST00000650755.1:c.*479G>T (TRNT1) ENSP00000499122.1:n.*479G>T
ENST00000650814.1:c.529G>T (TRNT1)
ENST00000650839.1:c.*201G>T (TRNT1) ENSP00000498970.1:n.*201G>T
ENST00000650989.1:n.376G>T (TRNT1)
ENST00000651093.1:c.*14G>T (TRNT1) ENSP00000498942.1:n.*14G>T
ENST00000651316.1:c.*174G>T (TRNT1) ENSP00000498787.1:n.*174G>T
ENST00000651352.1:c.*300G>T (TRNT1) ENSP00000498449.1:n.*300G>T
ENST00000651591.1:c.*559G>T (TRNT1) ENSP00000498240.1:n.*559G>T
ENST00000652340.1:c.622G>T (TRNT1) ENSP00000498624.1:n.622G>T
ENST00000698406.1:c.829G>T (TRNT1) ENSP00000513700.1:p.Glu277Ter
ENST00000698407.1:n.1458G>T (TRNT1)
ENST00000698408.1:c.829G>T (TRNT1) ENSP00000513701.1:p.Glu277Ter
ENST00000698410.1:c.*300G>T (TRNT1) ENSP00000513703.1:n.*300G>T
ENST00000698412.1:c.829G>T (TRNT1) ENSP00000513705.1:p.Glu277Ter
ENST00000698413.1:c.946G>T (TRNT1) ENSP00000513706.1:p.Glu316Ter
ENST00000698414.1:c.946G>T (TRNT1) ENSP00000513707.1:p.Glu316Ter
ENST00000698415.1:n.2190G>T (TRNT1)
ENST00000698416.1:n.1093G>T (TRNT1)
XM_005265196.1:c.829G>T (TRNT1) XP_005265253.1:p.Glu277Ter
XM_011533776.1:c.829G>T (TRNT1) XP_011532078.1:p.Glu277Ter
XM_011533776.3:c.829G>T (TRNT1) XP_011532078.1:p.Glu277Ter
XM_011533777.1:c.829G>T (TRNT1) XP_011532079.1:p.Glu277Ter
XM_011533777.2:c.829G>T (TRNT1) XP_011532079.1:p.Glu277Ter
XM_011533778.1:c.829G>T (TRNT1) XP_011532080.1:p.Glu277Ter
XM_011533778.3:c.829G>T (TRNT1) XP_011532080.1:p.Glu277Ter
XR_001740168.2:n.910G>T (TRNT1)
XR_001740169.2:n.910G>T (TRNT1)
XR_940445.1:n.931G>T (TRNT1)
XR_940445.3:n.910G>T (TRNT1)
XR_940446.1:n.931G>T (TRNT1)
XR_940446.3:n.910G>T (TRNT1)