Canonical Allele Identifier: CA1876848352
Gene: TRAF1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.120914118G= , CM000671.2:g.120914118G= GRCh38
NC_000009.11:g.123676396G= , CM000671.1:g.123676396G= GRCh37
NC_000009.10:g.122716217G= NCBI36
NG_023346.1:g.20056C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000373887.8:c.294+117C= MANE Select ENSP00000362994.3:n.294+117C=
ENST00000373887.7:c.294+117C= ENSP00000362994.3:n.294+117C=
ENST00000540010.1:c.294+117C= ENSP00000443183.1:n.294+117C=
ENST00000546084.5:c.-73+117C= ENSP00000438583.1:n.-73+117C=
NM_001190945.1:c.294+117C= NP_001177874.1:n.294+117C=
NM_001190947.1:c.-73+117C= NP_001177876.1:n.-73+117C=
NM_005658.4:c.294+117C= NP_005649.1:n.294+117C=
NM_005658.5:c.294+117C= MANE Select NP_005649.1:n.294+117C=
NM_001190945.2:c.294+117C= NP_001177874.1:n.294+117C=
NM_001190947.2:c.-73+117C= NP_001177876.1:n.-73+117C=