Canonical Allele Identifier: CA2839877226
Gene: TNFRSF1A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.6333834dup , CM000674.2:g.6333834dup GRCh38
NC_000012.11:g.6443000dup , CM000674.1:g.6443000dup GRCh37
NC_000012.10:g.6313261dup NCBI36
NG_007506.1:g.13265dup , LRG_193:g.13265dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000366159.9:n.262dup
ENST00000437813.8:c.228dup ENSP00000513672.1:p.Gln77AlafsTer9
ENST00000440083.7:c.228dup ENSP00000413224.3:p.Gln77AlafsTer9
ENST00000535958.2:c.*55dup ENSP00000513673.1:n.*55dup
ENST00000698339.1:c.228dup ENSP00000513670.1:p.Gln77AlafsTer9
ENST00000698340.1:c.228dup ENSP00000513671.1:p.Gln77AlafsTer9
ENST00000162749.7:c.228dup MANE Select ENSP00000162749.2:p.Gln77AlafsTer9
ENST00000162749.6:c.228dup ENSP00000162749.2:p.Gln77AlafsTer9
ENST00000366159.8:c.228dup ENSP00000380389.3:p.Gln77AlafsTer9
ENST00000437813.7:n.189dup
ENST00000440083.6:c.228dup ENSP00000413224.2:p.Gln77AlafsTer9
ENST00000534885.5:c.74dup ENSP00000441803.1:p.Arg26GlnfsTer?
ENST00000535958.1:n.474dup
ENST00000536194.1:c.201dup ENSP00000442919.1:p.Gln68AlafsTer9
ENST00000539372.5:c.228dup ENSP00000442059.1:p.Gln77AlafsTer9
ENST00000540022.5:c.193+260dup ENSP00000438343.1:n.193+260dup
ENST00000543048.5:c.214+14dup ENSP00000439981.1:n.214+14dup
ENST00000543995.5:c.193+260dup ENSP00000442405.1:n.193+260dup
NM_001065.3:c.228dup , LRG_193t1:c.228dup NP_001056.1:p.Gln77AlafsTer9
NM_001346091.1:c.-97dup NP_001333020.1:n.-97dup
NM_001346092.1:c.-350dup NP_001333021.1:n.-350dup
NR_144351.1:n.531dup
NM_001065.4:c.228dup MANE Select NP_001056.1:p.Gln77AlafsTer9
NM_001346091.2:c.-97dup NP_001333020.1:n.-97dup
NM_001346092.2:c.-350dup NP_001333021.1:n.-350dup
NR_144351.2:n.490dup