Canonical Allele Identifier: CA2617250876

Gene: TNFRSF1A

Linked Data

• gnomAD v4: 12-6330769-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6330769A>G , CM000674.2:g.6330769A>G	GRCh38
NC_000012.11:g.6439935A>G , CM000674.1:g.6439935A>G	GRCh37
NC_000012.10:g.6310196A>G	NCBI36
NG_007506.1:g.16327T>C , LRG_193:g.16327T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366159.9:n.1727-58T>C
ENST00000437813.8:c.*87-58T>C	ENSP00000513672.1:n.*87-58T>C
ENST00000440083.7:c.845-58T>C	ENSP00000413224.3:n.845-58T>C
ENST00000535038.2:n.808-58T>C
ENST00000535958.2:c.*453-58T>C	ENSP00000513673.1:n.*453-58T>C
ENST00000698337.1:n.558T>C
ENST00000698338.1:n.982T>C
ENST00000698339.1:c.*121-58T>C	ENSP00000513670.1:n.*121-58T>C
ENST00000698340.1:c.552-58T>C	ENSP00000513671.1:n.552-58T>C
ENST00000162749.7:c.626-58T>C MANE Select	ENSP00000162749.2:n.626-58T>C
ENST00000162749.6:c.626-58T>C	ENSP00000162749.2:n.626-58T>C
ENST00000534885.5:c.*103-58T>C	ENSP00000441803.1:n.*103-58T>C
ENST00000535038.1:n.379T>C
ENST00000536717.5:n.530-58T>C
ENST00000537842.5:n.230-58T>C
ENST00000539372.5:c.626-58T>C	ENSP00000442059.1:n.626-58T>C
ENST00000540022.5:c.497-58T>C	ENSP00000438343.1:n.497-58T>C
ENST00000543359.5:n.38-58T>C
ENST00000543995.5:c.*213-58T>C	ENSP00000442405.1:n.*213-58T>C
NM_001065.3:c.626-58T>C , LRG_193t1:c.626-58T>C	NP_001056.1:n.626-58T>C
NM_001346091.1:c.302-58T>C	NP_001333020.1:n.302-58T>C
NM_001346092.1:c.167-58T>C	NP_001333021.1:n.167-58T>C
NR_144351.1:n.855-58T>C
NM_001065.4:c.626-58T>C MANE Select	NP_001056.1:n.626-58T>C
NM_001346091.2:c.302-58T>C	NP_001333020.1:n.302-58T>C
NM_001346092.2:c.167-58T>C	NP_001333021.1:n.167-58T>C
NR_144351.2:n.814-58T>C