Canonical Allele Identifier: CA232325253

Gene: TNFRSF1A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6329060T>C , CM000674.2:g.6329060T>C	GRCh38
NC_000012.11:g.6438226T>C , CM000674.1:g.6438226T>C	GRCh37
NC_000012.10:g.6308487T>C	NCBI36
NG_007506.1:g.18036A>G , LRG_193:g.18036A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_001065.4:c.*252A>G MANE Select	NP_001056.1:n.*252A>G
ENST00000162749.7:c.*252A>G MANE Select	ENSP00000162749.2:n.*252A>G
NM_001065.3:c.*252A>G , LRG_193t1:c.*252A>G	NP_001056.1:n.*252A>G
NM_001346091.1:c.*252A>G	NP_001333020.1:n.*252A>G
NM_001346091.2:c.*252A>G	NP_001333020.1:n.*252A>G
NM_001346092.1:c.*252A>G	NP_001333021.1:n.*252A>G
NM_001346092.2:c.*252A>G	NP_001333021.1:n.*252A>G
NR_144351.1:n.1849A>G
NR_144351.2:n.1808A>G
ENST00000162749.6:c.*252A>G	ENSP00000162749.2:n.*252A>G
ENST00000366159.9:n.2721A>G
ENST00000437813.8:c.*1081A>G	ENSP00000513672.1:n.*1081A>G
ENST00000440083.7:c.*252A>G	ENSP00000413224.3:n.*252A>G
ENST00000534885.5:c.*1097A>G	ENSP00000441803.1:n.*1097A>G
ENST00000535958.2:c.*1447A>G	ENSP00000513673.1:n.*1447A>G
ENST00000698337.1:n.1581A>G
ENST00000698338.1:n.2234A>G
ENST00000698339.1:c.*1115A>G	ENSP00000513670.1:n.*1115A>G
ENST00000698340.1:c.*859A>G	ENSP00000513671.1:n.*859A>G