Canonical Allele Identifier: CA690827616

Gene: TNFRSF1A

Linked Data

• dbSNP Id: rs1235555649
• gnomAD v3: 12-6330748-A-C
• gnomAD v4: 12-6330748-A-C
• MyVariant Identifiers: chr12:g.6439914A>C (hg19) ; chr12:g.6330748A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6330748A>C , CM000674.2:g.6330748A>C	GRCh38
NC_000012.11:g.6439914A>C , CM000674.1:g.6439914A>C	GRCh37
NC_000012.10:g.6310175A>C	NCBI36
NG_007506.1:g.16348T>G , LRG_193:g.16348T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366159.9:n.1727-37T>G
ENST00000437813.8:c.*87-37T>G	ENSP00000513672.1:n.*87-37T>G
ENST00000440083.7:c.845-37T>G	ENSP00000413224.3:n.845-37T>G
ENST00000535038.2:n.808-37T>G
ENST00000535958.2:c.*453-37T>G	ENSP00000513673.1:n.*453-37T>G
ENST00000698337.1:n.579T>G
ENST00000698338.1:n.1003T>G
ENST00000698339.1:c.*121-37T>G	ENSP00000513670.1:n.*121-37T>G
ENST00000698340.1:c.552-37T>G	ENSP00000513671.1:n.552-37T>G
ENST00000162749.7:c.626-37T>G MANE Select	ENSP00000162749.2:n.626-37T>G
ENST00000162749.6:c.626-37T>G	ENSP00000162749.2:n.626-37T>G
ENST00000534885.5:c.*103-37T>G	ENSP00000441803.1:n.*103-37T>G
ENST00000535038.1:n.400T>G
ENST00000536717.5:n.530-37T>G
ENST00000537842.5:n.230-37T>G
ENST00000539372.5:c.626-37T>G	ENSP00000442059.1:n.626-37T>G
ENST00000540022.5:c.497-37T>G	ENSP00000438343.1:n.497-37T>G
ENST00000543359.5:n.38-37T>G
ENST00000543995.5:c.*213-37T>G	ENSP00000442405.1:n.*213-37T>G
NM_001065.3:c.626-37T>G , LRG_193t1:c.626-37T>G	NP_001056.1:n.626-37T>G
NM_001346091.1:c.302-37T>G	NP_001333020.1:n.302-37T>G
NM_001346092.1:c.167-37T>G	NP_001333021.1:n.167-37T>G
NR_144351.1:n.855-37T>G
NM_001065.4:c.626-37T>G MANE Select	NP_001056.1:n.626-37T>G
NM_001346091.2:c.302-37T>G	NP_001333020.1:n.302-37T>G
NM_001346092.2:c.167-37T>G	NP_001333021.1:n.167-37T>G
NR_144351.2:n.814-37T>G