Canonical Allele Identifier: CA2617248834

Gene: TNFRSF1A

Linked Data

• gnomAD v4: 12-6329722-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6329722C>A , CM000674.2:g.6329722C>A	GRCh38
NC_000012.11:g.6438888C>A , CM000674.1:g.6438888C>A	GRCh37
NC_000012.10:g.6309149C>A	NCBI36
NG_007506.1:g.17374G>T , LRG_193:g.17374G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366159.9:n.2158+56G>T
ENST00000437813.8:c.*518+56G>T	ENSP00000513672.1:n.*518+56G>T
ENST00000440083.7:c.1276+56G>T	ENSP00000413224.3:n.1276+56G>T
ENST00000535958.2:c.*884+56G>T	ENSP00000513673.1:n.*884+56G>T
ENST00000698337.1:n.1018+56G>T
ENST00000698338.1:n.1671+56G>T
ENST00000698339.1:c.*552+56G>T	ENSP00000513670.1:n.*552+56G>T
ENST00000698340.1:c.*296+56G>T	ENSP00000513671.1:n.*296+56G>T
ENST00000162749.7:c.1057+56G>T MANE Select	ENSP00000162749.2:n.1057+56G>T
ENST00000162749.6:c.1057+56G>T	ENSP00000162749.2:n.1057+56G>T
ENST00000534885.5:c.*534+56G>T	ENSP00000441803.1:n.*534+56G>T
ENST00000536717.5:n.961+56G>T
ENST00000540022.5:c.928+56G>T	ENSP00000438343.1:n.928+56G>T
ENST00000543359.5:n.469+56G>T
ENST00000543995.5:c.*644+56G>T	ENSP00000442405.1:n.*644+56G>T
NM_001065.3:c.1057+56G>T , LRG_193t1:c.1057+56G>T	NP_001056.1:n.1057+56G>T
NM_001346091.1:c.733+56G>T	NP_001333020.1:n.733+56G>T
NM_001346092.1:c.598+56G>T	NP_001333021.1:n.598+56G>T
NR_144351.1:n.1286+56G>T
NM_001065.4:c.1057+56G>T MANE Select	NP_001056.1:n.1057+56G>T
NM_001346091.2:c.733+56G>T	NP_001333020.1:n.733+56G>T
NM_001346092.2:c.598+56G>T	NP_001333021.1:n.598+56G>T
NR_144351.2:n.1245+56G>T