Canonical Allele Identifier: CA383545904

Gene: TNFRSF1A

Linked Data

• MyVariant Identifiers: chr12:g.6439087G>T (hg19) ; chr12:g.6329921G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6329921G>T , CM000674.2:g.6329921G>T	GRCh38
NC_000012.11:g.6439087G>T , CM000674.1:g.6439087G>T	GRCh37
NC_000012.10:g.6309348G>T	NCBI36
NG_007506.1:g.17175C>A , LRG_193:g.17175C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000366159.9:n.2015C>A
ENST00000437813.8:c.*375C>A	ENSP00000513672.1:n.*375C>A
ENST00000440083.7:c.1133C>A	ENSP00000413224.3:p.Pro378His
ENST00000535958.2:c.*741C>A	ENSP00000513673.1:n.*741C>A
ENST00000698337.1:n.875C>A
ENST00000698338.1:n.1528C>A
ENST00000698339.1:c.*409C>A	ENSP00000513670.1:n.*409C>A
ENST00000698340.1:c.*153C>A	ENSP00000513671.1:n.*153C>A
ENST00000162749.7:c.914C>A MANE Select	ENSP00000162749.2:p.Pro305His
ENST00000162749.6:c.914C>A	ENSP00000162749.2:p.Pro305His
ENST00000534885.5:c.*391C>A	ENSP00000441803.1:n.*391C>A
ENST00000536717.5:n.818C>A
ENST00000537842.5:n.373-22C>A
ENST00000540022.5:c.785C>A	ENSP00000438343.1:p.Pro262His
ENST00000543359.5:n.326C>A
ENST00000543995.5:c.*501C>A	ENSP00000442405.1:n.*501C>A
NM_001065.3:c.914C>A , LRG_193t1:c.914C>A	NP_001056.1:p.Pro305His
NM_001346091.1:c.590C>A	NP_001333020.1:p.Pro197His
NM_001346092.1:c.455C>A	NP_001333021.1:p.Pro152His
NR_144351.1:n.1143C>A
NM_001065.4:c.914C>A MANE Select	NP_001056.1:p.Pro305His
NM_001346091.2:c.590C>A	NP_001333020.1:p.Pro197His
NM_001346092.2:c.455C>A	NP_001333021.1:p.Pro152His
NR_144351.2:n.1102C>A