Canonical Allele Identifier: CA383549007

Gene: TNFRSF1A

Linked Data

• MyVariant Identifiers: chr12:g.6442245A>C (hg19) ; chr12:g.6333079A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6333079A>C , CM000674.2:g.6333079A>C	GRCh38
NC_000012.11:g.6442245A>C , CM000674.1:g.6442245A>C	GRCh37
NC_000012.10:g.6312506A>C	NCBI36
NG_007506.1:g.14017T>G , LRG_193:g.14017T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366159.9:n.575T>G
ENST00000437813.8:c.541T>G	ENSP00000513672.1:p.Ser181Ala
ENST00000440083.7:c.760T>G	ENSP00000413224.3:p.Ser254Ala
ENST00000535958.2:c.*368T>G	ENSP00000513673.1:n.*368T>G
ENST00000698339.1:c.541T>G	ENSP00000513670.1:p.Ser181Ala
ENST00000698340.1:c.541T>G	ENSP00000513671.1:p.Ser181Ala
ENST00000162749.7:c.541T>G MANE Select	ENSP00000162749.2:p.Ser181Ala
ENST00000162749.6:c.541T>G	ENSP00000162749.2:p.Ser181Ala
ENST00000366159.8:c.541T>G	ENSP00000380389.3:p.Ser181Ala
ENST00000437813.7:n.502T>G
ENST00000440083.6:c.760T>G	ENSP00000413224.2:p.Ser254Ala
ENST00000534885.5:c.*18T>G	ENSP00000441803.1:n.*18T>G
ENST00000537842.5:n.145T>G
ENST00000539372.5:c.541T>G	ENSP00000442059.1:p.Ser181Ala
ENST00000540022.5:c.412T>G	ENSP00000438343.1:p.Ser138Ala
ENST00000543048.5:c.*152T>G	ENSP00000439981.1:n.*152T>G
ENST00000543359.5:n.27T>G
ENST00000543995.5:c.*128T>G	ENSP00000442405.1:n.*128T>G
NM_001065.3:c.541T>G , LRG_193t1:c.541T>G	NP_001056.1:p.Ser181Ala
NM_001346091.1:c.217T>G	NP_001333020.1:p.Ser73Ala
NM_001346092.1:c.-37T>G	NP_001333021.1:n.-37T>G
NR_144351.1:n.844T>G
NM_001065.4:c.541T>G MANE Select	NP_001056.1:p.Ser181Ala
NM_001346091.2:c.217T>G	NP_001333020.1:p.Ser73Ala
NM_001346092.2:c.-37T>G	NP_001333021.1:n.-37T>G
NR_144351.2:n.803T>G