Canonical Allele Identifier: CA383550070

Gene: TNFRSF1A

Linked Data

• MyVariant Identifiers: chr12:g.6442600A>C (hg19) ; chr12:g.6333434A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6333434A>C , CM000674.2:g.6333434A>C	GRCh38
NC_000012.11:g.6442600A>C , CM000674.1:g.6442600A>C	GRCh37
NC_000012.10:g.6312861A>C	NCBI36
NG_007506.1:g.13662T>G , LRG_193:g.13662T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366159.9:n.439T>G
ENST00000437813.8:c.405T>G	ENSP00000513672.1:p.Tyr135Ter
ENST00000440083.7:c.405T>G	ENSP00000413224.3:p.Tyr135Ter
ENST00000535958.2:c.*232T>G	ENSP00000513673.1:n.*232T>G
ENST00000698339.1:c.405T>G	ENSP00000513670.1:p.Tyr135Ter
ENST00000698340.1:c.405T>G	ENSP00000513671.1:p.Tyr135Ter
ENST00000162749.7:c.405T>G MANE Select	ENSP00000162749.2:p.Tyr135Ter
ENST00000162749.6:c.405T>G	ENSP00000162749.2:p.Tyr135Ter
ENST00000366159.8:c.405T>G	ENSP00000380389.3:p.Tyr135Ter
ENST00000437813.7:n.366T>G
ENST00000440083.6:c.405T>G	ENSP00000413224.2:p.Tyr135Ter
ENST00000534885.5:c.251T>G	ENSP00000441803.1:p.Ile84Ser
ENST00000537842.5:n.9T>G
ENST00000539372.5:c.405T>G	ENSP00000442059.1:p.Tyr135Ter
ENST00000540022.5:c.276T>G	ENSP00000438343.1:p.Tyr92Ter
ENST00000543048.5:c.*16T>G	ENSP00000439981.1:n.*16T>G
ENST00000543995.5:c.211T>G	ENSP00000442405.1:p.Leu71Val
NM_001065.3:c.405T>G , LRG_193t1:c.405T>G	NP_001056.1:p.Tyr135Ter
NM_001346091.1:c.81T>G	NP_001333020.1:p.Tyr27Ter
NM_001346092.1:c.-173T>G	NP_001333021.1:n.-173T>G
NR_144351.1:n.708T>G
NM_001065.4:c.405T>G MANE Select	NP_001056.1:p.Tyr135Ter
NM_001346091.2:c.81T>G	NP_001333020.1:p.Tyr27Ter
NM_001346092.2:c.-173T>G	NP_001333021.1:n.-173T>G
NR_144351.2:n.667T>G