Canonical Allele Identifier: CA232326332

Gene: TNFRSF1A

Linked Data

• dbSNP Id: rs1804532
• gnomAD v4: 12-6329922-G-T
• MyVariant Identifiers: chr12:g.6439088G>T (hg19) ; chr12:g.6329922G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6329922G>T , CM000674.2:g.6329922G>T	GRCh38
NC_000012.11:g.6439088G>T , CM000674.1:g.6439088G>T	GRCh37
NC_000012.10:g.6309349G>T	NCBI36
NG_007506.1:g.17174C>A , LRG_193:g.17174C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366159.9:n.2014C>A
ENST00000437813.8:c.*374C>A	ENSP00000513672.1:n.*374C>A
ENST00000440083.7:c.1132C>A	ENSP00000413224.3:p.Pro378Thr
ENST00000535958.2:c.*740C>A	ENSP00000513673.1:n.*740C>A
ENST00000698337.1:n.874C>A
ENST00000698338.1:n.1527C>A
ENST00000698339.1:c.*408C>A	ENSP00000513670.1:n.*408C>A
ENST00000698340.1:c.*152C>A	ENSP00000513671.1:n.*152C>A
ENST00000162749.7:c.913C>A MANE Select	ENSP00000162749.2:p.Pro305Thr
ENST00000162749.6:c.913C>A	ENSP00000162749.2:p.Pro305Thr
ENST00000534885.5:c.*390C>A	ENSP00000441803.1:n.*390C>A
ENST00000536717.5:n.817C>A
ENST00000537842.5:n.373-23C>A
ENST00000540022.5:c.784C>A	ENSP00000438343.1:p.Pro262Thr
ENST00000543359.5:n.325C>A
ENST00000543995.5:c.*500C>A	ENSP00000442405.1:n.*500C>A
NM_001065.3:c.913C>A , LRG_193t1:c.913C>A	NP_001056.1:p.Pro305Thr
NM_001346091.1:c.589C>A	NP_001333020.1:p.Pro197Thr
NM_001346092.1:c.454C>A	NP_001333021.1:p.Pro152Thr
NR_144351.1:n.1142C>A
NM_001065.4:c.913C>A MANE Select	NP_001056.1:p.Pro305Thr
NM_001346091.2:c.589C>A	NP_001333020.1:p.Pro197Thr
NM_001346092.2:c.454C>A	NP_001333021.1:p.Pro152Thr
NR_144351.2:n.1101C>A