Canonical Allele Identifier: CA2014026176
Gene: TNFRSF1A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.6333684G= , CM000674.2:g.6333684G= GRCh38
NC_000012.11:g.6442850G= , CM000674.1:g.6442850G= GRCh37
NC_000012.10:g.6313111G= NCBI36
NG_007506.1:g.13412C= , LRG_193:g.13412C=

Transcript Alleles

HGVS Amino-acid change
ENST00000366159.9:n.356+53C=
ENST00000437813.8:c.322+53C= ENSP00000513672.1:n.322+53C=
ENST00000440083.7:c.322+53C= ENSP00000413224.3:n.322+53C=
ENST00000535958.2:c.*149+53C= ENSP00000513673.1:n.*149+53C=
ENST00000698339.1:c.322+53C= ENSP00000513670.1:n.322+53C=
ENST00000698340.1:c.322+53C= ENSP00000513671.1:n.322+53C=
ENST00000162749.7:c.322+53C= MANE Select ENSP00000162749.2:n.322+53C=
ENST00000162749.6:c.322+53C= ENSP00000162749.2:n.322+53C=
ENST00000366159.8:c.322+53C= ENSP00000380389.3:n.322+53C=
ENST00000437813.7:n.283+53C=
ENST00000440083.6:c.322+53C= ENSP00000413224.2:n.322+53C=
ENST00000534885.5:c.168+53C= ENSP00000441803.1:n.168+53C=
ENST00000536194.1:c.295+53C= ENSP00000442919.1:n.295+53C=
ENST00000539372.5:c.322+53C= ENSP00000442059.1:n.322+53C=
ENST00000540022.5:c.194-168C= ENSP00000438343.1:n.194-168C=
ENST00000543048.5:c.214+161C= ENSP00000439981.1:n.214+161C=
ENST00000543995.5:c.194-233C= ENSP00000442405.1:n.194-233C=
NM_001065.3:c.322+53C= , LRG_193t1:c.322+53C= NP_001056.1:n.322+53C=
NM_001346091.1:c.-3+53C= NP_001333020.1:n.-3+53C=
NM_001346092.1:c.-256+53C= NP_001333021.1:n.-256+53C=
NR_144351.1:n.625+53C=
NM_001065.4:c.322+53C= MANE Select NP_001056.1:n.322+53C=
NM_001346091.2:c.-3+53C= NP_001333020.1:n.-3+53C=
NM_001346092.2:c.-256+53C= NP_001333021.1:n.-256+53C=
NR_144351.2:n.584+53C=