Canonical Allele Identifier: CA2014024090
Gene: TNFRSF1A HGNC NCBI

Linked Data

dbSNP Id: rs1948039493

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.6330745G>A , CM000674.2:g.6330745G>A GRCh38
NC_000012.11:g.6439911G>A , CM000674.1:g.6439911G>A GRCh37
NC_000012.10:g.6310172G>A NCBI36
NG_007506.1:g.16351C>T , LRG_193:g.16351C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000366159.9:n.1727-34C>T
ENST00000437813.8:c.*87-34C>T ENSP00000513672.1:n.*87-34C>T
ENST00000440083.7:c.845-34C>T ENSP00000413224.3:n.845-34C>T
ENST00000535038.2:n.808-34C>T
ENST00000535958.2:c.*453-34C>T ENSP00000513673.1:n.*453-34C>T
ENST00000698337.1:n.582C>T
ENST00000698338.1:n.1006C>T
ENST00000698339.1:c.*121-34C>T ENSP00000513670.1:n.*121-34C>T
ENST00000698340.1:c.552-34C>T ENSP00000513671.1:n.552-34C>T
ENST00000162749.7:c.626-34C>T MANE Select ENSP00000162749.2:n.626-34C>T
ENST00000162749.6:c.626-34C>T ENSP00000162749.2:n.626-34C>T
ENST00000534885.5:c.*103-34C>T ENSP00000441803.1:n.*103-34C>T
ENST00000535038.1:n.403C>T
ENST00000536717.5:n.530-34C>T
ENST00000537842.5:n.230-34C>T
ENST00000539372.5:c.626-34C>T ENSP00000442059.1:n.626-34C>T
ENST00000540022.5:c.497-34C>T ENSP00000438343.1:n.497-34C>T
ENST00000543359.5:n.38-34C>T
ENST00000543995.5:c.*213-34C>T ENSP00000442405.1:n.*213-34C>T
NM_001065.3:c.626-34C>T , LRG_193t1:c.626-34C>T NP_001056.1:n.626-34C>T
NM_001346091.1:c.302-34C>T NP_001333020.1:n.302-34C>T
NM_001346092.1:c.167-34C>T NP_001333021.1:n.167-34C>T
NR_144351.1:n.855-34C>T
NM_001065.4:c.626-34C>T MANE Select NP_001056.1:n.626-34C>T
NM_001346091.2:c.302-34C>T NP_001333020.1:n.302-34C>T
NM_001346092.2:c.167-34C>T NP_001333021.1:n.167-34C>T
NR_144351.2:n.814-34C>T