Canonical Allele Identifier: CA6405282

Gene: TNFRSF1A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6329653C>T , CM000674.2:g.6329653C>T	GRCh38
NC_000012.11:g.6438819C>T , CM000674.1:g.6438819C>T	GRCh37
NC_000012.10:g.6309080C>T	NCBI36
NG_007506.1:g.17443G>A , LRG_193:g.17443G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001065.4:c.1058-31G>A MANE Select	NP_001056.1:n.1058-31G>A
ENST00000162749.7:c.1058-31G>A MANE Select	ENSP00000162749.2:n.1058-31G>A
NM_001065.3:c.1058-31G>A , LRG_193t1:c.1058-31G>A	NP_001056.1:n.1058-31G>A
NM_001346091.1:c.734-31G>A	NP_001333020.1:n.734-31G>A
NM_001346091.2:c.734-31G>A	NP_001333020.1:n.734-31G>A
NM_001346092.1:c.599-31G>A	NP_001333021.1:n.599-31G>A
NM_001346092.2:c.599-31G>A	NP_001333021.1:n.599-31G>A
NR_144351.1:n.1287-31G>A
NR_144351.2:n.1246-31G>A
ENST00000162749.6:c.1058-31G>A	ENSP00000162749.2:n.1058-31G>A
ENST00000366159.9:n.2159-31G>A
ENST00000437813.8:c.*519-31G>A	ENSP00000513672.1:n.*519-31G>A
ENST00000440083.7:c.1277-31G>A	ENSP00000413224.3:n.1277-31G>A
ENST00000534885.5:c.*535-31G>A	ENSP00000441803.1:n.*535-31G>A
ENST00000535958.2:c.*885-31G>A	ENSP00000513673.1:n.*885-31G>A
ENST00000536717.5:n.962-31G>A
ENST00000540022.5:c.929-31G>A	ENSP00000438343.1:n.929-31G>A
ENST00000543359.5:n.470-31G>A
ENST00000543995.5:c.*645-31G>A	ENSP00000442405.1:n.*645-31G>A
ENST00000698337.1:n.1019-31G>A
ENST00000698338.1:n.1672-31G>A
ENST00000698339.1:c.*553-31G>A	ENSP00000513670.1:n.*553-31G>A
ENST00000698340.1:c.*297-31G>A	ENSP00000513671.1:n.*297-31G>A