Canonical Allele Identifier: CA383546969

Gene: TNFRSF1A

Linked Data

• MyVariant Identifiers: chr12:g.6439767T>C (hg19) ; chr12:g.6330601T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6330601T>C , CM000674.2:g.6330601T>C	GRCh38
NC_000012.11:g.6439767T>C , CM000674.1:g.6439767T>C	GRCh37
NC_000012.10:g.6310028T>C	NCBI36
NG_007506.1:g.16495A>G , LRG_193:g.16495A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366159.9:n.1837A>G
ENST00000437813.8:c.*197A>G	ENSP00000513672.1:n.*197A>G
ENST00000440083.7:c.955A>G	ENSP00000413224.3:p.Ile319Val
ENST00000535038.2:n.918A>G
ENST00000535958.2:c.*563A>G	ENSP00000513673.1:n.*563A>G
ENST00000698337.1:n.726A>G
ENST00000698338.1:n.1150A>G
ENST00000698339.1:c.*231A>G	ENSP00000513670.1:n.*231A>G
ENST00000698340.1:c.662A>G	ENSP00000513671.1:p.His221Arg
ENST00000162749.7:c.736A>G MANE Select	ENSP00000162749.2:p.Ile246Val
ENST00000162749.6:c.736A>G	ENSP00000162749.2:p.Ile246Val
ENST00000534885.5:c.*213A>G	ENSP00000441803.1:n.*213A>G
ENST00000535038.1:n.547A>G
ENST00000536717.5:n.640A>G
ENST00000537842.5:n.340A>G
ENST00000539372.5:c.736A>G	ENSP00000442059.1:p.Ile246Val
ENST00000540022.5:c.607A>G	ENSP00000438343.1:p.Ile203Val
ENST00000543359.5:n.148A>G
ENST00000543995.5:c.*323A>G	ENSP00000442405.1:n.*323A>G
NM_001065.3:c.736A>G , LRG_193t1:c.736A>G	NP_001056.1:p.Ile246Val
NM_001346091.1:c.412A>G	NP_001333020.1:p.Ile138Val
NM_001346092.1:c.277A>G	NP_001333021.1:p.Ile93Val
NR_144351.1:n.965A>G
NM_001065.4:c.736A>G MANE Select	NP_001056.1:p.Ile246Val
NM_001346091.2:c.412A>G	NP_001333020.1:p.Ile138Val
NM_001346092.2:c.277A>G	NP_001333021.1:p.Ile93Val
NR_144351.2:n.924A>G