Canonical Allele Identifier: CA6405305

Gene: TNFRSF1A

Linked Data

• dbSNP Id: rs753389605
• ExAC: 12:6438980 A / C
• gnomAD v4: 12-6329814-A-C
• MyVariant Identifiers: chr12:g.6438980A>C (hg19) ; chr12:g.6329814A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6329814A>C , CM000674.2:g.6329814A>C	GRCh38
NC_000012.11:g.6438980A>C , CM000674.1:g.6438980A>C	GRCh37
NC_000012.10:g.6309241A>C	NCBI36
NG_007506.1:g.17282T>G , LRG_193:g.17282T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000366159.9:n.2122T>G
ENST00000437813.8:c.*482T>G	ENSP00000513672.1:n.*482T>G
ENST00000440083.7:c.1240T>G	ENSP00000413224.3:p.Trp414Gly
ENST00000535958.2:c.*848T>G	ENSP00000513673.1:n.*848T>G
ENST00000698337.1:n.982T>G
ENST00000698338.1:n.1635T>G
ENST00000698339.1:c.*516T>G	ENSP00000513670.1:n.*516T>G
ENST00000698340.1:c.*260T>G	ENSP00000513671.1:n.*260T>G
ENST00000162749.7:c.1021T>G MANE Select	ENSP00000162749.2:p.Trp341Gly
ENST00000162749.6:c.1021T>G	ENSP00000162749.2:p.Trp341Gly
ENST00000534885.5:c.*498T>G	ENSP00000441803.1:n.*498T>G
ENST00000536717.5:n.925T>G
ENST00000540022.5:c.892T>G	ENSP00000438343.1:p.Trp298Gly
ENST00000543359.5:n.433T>G
ENST00000543995.5:c.*608T>G	ENSP00000442405.1:n.*608T>G
NM_001065.3:c.1021T>G , LRG_193t1:c.1021T>G	NP_001056.1:p.Trp341Gly
NM_001346091.1:c.697T>G	NP_001333020.1:p.Trp233Gly
NM_001346092.1:c.562T>G	NP_001333021.1:p.Trp188Gly
NR_144351.1:n.1250T>G
NM_001065.4:c.1021T>G MANE Select	NP_001056.1:p.Trp341Gly
NM_001346091.2:c.697T>G	NP_001333020.1:p.Trp233Gly
NM_001346092.2:c.562T>G	NP_001333021.1:p.Trp188Gly
NR_144351.2:n.1209T>G