Canonical Allele Identifier: CA383546962

Gene: TNFRSF1A

Linked Data

• MyVariant Identifiers: chr12:g.6439765A>C (hg19) ; chr12:g.6330599A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6330599A>C , CM000674.2:g.6330599A>C	GRCh38
NC_000012.11:g.6439765A>C , CM000674.1:g.6439765A>C	GRCh37
NC_000012.10:g.6310026A>C	NCBI36
NG_007506.1:g.16497T>G , LRG_193:g.16497T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366159.9:n.1839T>G
ENST00000437813.8:c.*199T>G	ENSP00000513672.1:n.*199T>G
ENST00000440083.7:c.957T>G	ENSP00000413224.3:p.Ile319Met
ENST00000535038.2:n.920T>G
ENST00000535958.2:c.*565T>G	ENSP00000513673.1:n.*565T>G
ENST00000698337.1:n.728T>G
ENST00000698338.1:n.1152T>G
ENST00000698339.1:c.*233T>G	ENSP00000513670.1:n.*233T>G
ENST00000698340.1:c.664T>G	ENSP00000513671.1:p.Cys222Gly
ENST00000162749.7:c.738T>G MANE Select	ENSP00000162749.2:p.Ile246Met
ENST00000162749.6:c.738T>G	ENSP00000162749.2:p.Ile246Met
ENST00000534885.5:c.*215T>G	ENSP00000441803.1:n.*215T>G
ENST00000535038.1:n.549T>G
ENST00000536717.5:n.642T>G
ENST00000537842.5:n.342T>G
ENST00000539372.5:c.738T>G	ENSP00000442059.1:p.Ile246Met
ENST00000540022.5:c.609T>G	ENSP00000438343.1:p.Ile203Met
ENST00000543359.5:n.150T>G
ENST00000543995.5:c.*325T>G	ENSP00000442405.1:n.*325T>G
NM_001065.3:c.738T>G , LRG_193t1:c.738T>G	NP_001056.1:p.Ile246Met
NM_001346091.1:c.414T>G	NP_001333020.1:p.Ile138Met
NM_001346092.1:c.279T>G	NP_001333021.1:p.Ile93Met
NR_144351.1:n.967T>G
NM_001065.4:c.738T>G MANE Select	NP_001056.1:p.Ile246Met
NM_001346091.2:c.414T>G	NP_001333020.1:p.Ile138Met
NM_001346092.2:c.279T>G	NP_001333021.1:p.Ile93Met
NR_144351.2:n.926T>G