Canonical Allele Identifier: CA383550560

Gene: TNFRSF1A

Linked Data

• MyVariant Identifiers: chr12:g.6442963A>C (hg19) ; chr12:g.6333797A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6333797A>C , CM000674.2:g.6333797A>C	GRCh38
NC_000012.11:g.6442963A>C , CM000674.1:g.6442963A>C	GRCh37
NC_000012.10:g.6313224A>C	NCBI36
NG_007506.1:g.13299T>G , LRG_193:g.13299T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366159.9:n.296T>G
ENST00000437813.8:c.262T>G	ENSP00000513672.1:p.Ser88Ala
ENST00000440083.7:c.262T>G	ENSP00000413224.3:p.Ser88Ala
ENST00000535958.2:c.*89T>G	ENSP00000513673.1:n.*89T>G
ENST00000698339.1:c.262T>G	ENSP00000513670.1:p.Ser88Ala
ENST00000698340.1:c.262T>G	ENSP00000513671.1:p.Ser88Ala
ENST00000162749.7:c.262T>G MANE Select	ENSP00000162749.2:p.Ser88Ala
ENST00000162749.6:c.262T>G	ENSP00000162749.2:p.Ser88Ala
ENST00000366159.8:c.262T>G	ENSP00000380389.3:p.Ser88Ala
ENST00000437813.7:n.223T>G
ENST00000440083.6:c.262T>G	ENSP00000413224.2:p.Ser88Ala
ENST00000534885.5:c.108T>G	ENSP00000441803.1:p.Ala36=
ENST00000535958.1:n.508T>G
ENST00000536194.1:c.235T>G	ENSP00000442919.1:p.Ser79Ala
ENST00000539372.5:c.262T>G	ENSP00000442059.1:p.Ser88Ala
ENST00000540022.5:c.194-281T>G	ENSP00000438343.1:n.194-281T>G
ENST00000543048.5:c.214+48T>G	ENSP00000439981.1:n.214+48T>G
ENST00000543995.5:c.193+294T>G	ENSP00000442405.1:n.193+294T>G
NM_001065.3:c.262T>G , LRG_193t1:c.262T>G	NP_001056.1:p.Ser88Ala
NM_001346091.1:c.-63T>G	NP_001333020.1:n.-63T>G
NM_001346092.1:c.-316T>G	NP_001333021.1:n.-316T>G
NR_144351.1:n.565T>G
NM_001065.4:c.262T>G MANE Select	NP_001056.1:p.Ser88Ala
NM_001346091.2:c.-63T>G	NP_001333020.1:n.-63T>G
NM_001346092.2:c.-316T>G	NP_001333021.1:n.-316T>G
NR_144351.2:n.524T>G