Canonical Allele Identifier: CA383548076

Gene: TNFRSF1A

Linked Data

• MyVariant Identifiers: chr12:g.6440059G>C (hg19) ; chr12:g.6330893G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6330893G>C , CM000674.2:g.6330893G>C	GRCh38
NC_000012.11:g.6440059G>C , CM000674.1:g.6440059G>C	GRCh37
NC_000012.10:g.6310320G>C	NCBI36
NG_007506.1:g.16203C>G , LRG_193:g.16203C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366159.9:n.1686C>G
ENST00000437813.8:c.*46C>G	ENSP00000513672.1:n.*46C>G
ENST00000440083.7:c.804C>G	ENSP00000413224.3:p.Cys268Trp
ENST00000535038.2:n.767C>G
ENST00000535958.2:c.*412C>G	ENSP00000513673.1:n.*412C>G
ENST00000698337.1:n.434C>G
ENST00000698338.1:n.858C>G
ENST00000698339.1:c.*80C>G	ENSP00000513670.1:n.*80C>G
ENST00000698340.1:c.552-182C>G	ENSP00000513671.1:n.552-182C>G
ENST00000162749.7:c.585C>G MANE Select	ENSP00000162749.2:p.Cys195Trp
ENST00000162749.6:c.585C>G	ENSP00000162749.2:p.Cys195Trp
ENST00000534885.5:c.*62C>G	ENSP00000441803.1:n.*62C>G
ENST00000535038.1:n.255C>G
ENST00000536717.5:n.489C>G
ENST00000537842.5:n.189C>G
ENST00000539372.5:c.585C>G	ENSP00000442059.1:p.Cys195Trp
ENST00000540022.5:c.456C>G	ENSP00000438343.1:p.Cys152Trp
ENST00000543359.5:n.38-182C>G
ENST00000543995.5:c.*172C>G	ENSP00000442405.1:n.*172C>G
NM_001065.3:c.585C>G , LRG_193t1:c.585C>G	NP_001056.1:p.Cys195Trp
NM_001346091.1:c.261C>G	NP_001333020.1:p.Cys87Trp
NM_001346092.1:c.126C>G	NP_001333021.1:p.Cys42Trp
NR_144351.1:n.855-182C>G
NM_001065.4:c.585C>G MANE Select	NP_001056.1:p.Cys195Trp
NM_001346091.2:c.261C>G	NP_001333020.1:p.Cys87Trp
NM_001346092.2:c.126C>G	NP_001333021.1:p.Cys42Trp
NR_144351.2:n.814-182C>G