Canonical Allele Identifier: CA383545894

Gene: TNFRSF1A

Linked Data

• MyVariant Identifiers: chr12:g.6439084T>C (hg19) ; chr12:g.6329918T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6329918T>C , CM000674.2:g.6329918T>C	GRCh38
NC_000012.11:g.6439084T>C , CM000674.1:g.6439084T>C	GRCh37
NC_000012.10:g.6309345T>C	NCBI36
NG_007506.1:g.17178A>G , LRG_193:g.17178A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000366159.9:n.2018A>G
ENST00000437813.8:c.*378A>G	ENSP00000513672.1:n.*378A>G
ENST00000440083.7:c.1136A>G	ENSP00000413224.3:p.Asn379Ser
ENST00000535958.2:c.*744A>G	ENSP00000513673.1:n.*744A>G
ENST00000698337.1:n.878A>G
ENST00000698338.1:n.1531A>G
ENST00000698339.1:c.*412A>G	ENSP00000513670.1:n.*412A>G
ENST00000698340.1:c.*156A>G	ENSP00000513671.1:n.*156A>G
ENST00000162749.7:c.917A>G MANE Select	ENSP00000162749.2:p.Asn306Ser
ENST00000162749.6:c.917A>G	ENSP00000162749.2:p.Asn306Ser
ENST00000534885.5:c.*394A>G	ENSP00000441803.1:n.*394A>G
ENST00000536717.5:n.821A>G
ENST00000537842.5:n.373-19A>G
ENST00000540022.5:c.788A>G	ENSP00000438343.1:p.Asn263Ser
ENST00000543359.5:n.329A>G
ENST00000543995.5:c.*504A>G	ENSP00000442405.1:n.*504A>G
NM_001065.3:c.917A>G , LRG_193t1:c.917A>G	NP_001056.1:p.Asn306Ser
NM_001346091.1:c.593A>G	NP_001333020.1:p.Asn198Ser
NM_001346092.1:c.458A>G	NP_001333021.1:p.Asn153Ser
NR_144351.1:n.1146A>G
NM_001065.4:c.917A>G MANE Select	NP_001056.1:p.Asn306Ser
NM_001346091.2:c.593A>G	NP_001333020.1:p.Asn198Ser
NM_001346092.2:c.458A>G	NP_001333021.1:p.Asn153Ser
NR_144351.2:n.1105A>G