Canonical Allele Identifier: CA2617250867

Gene: TNFRSF1A

Linked Data

• gnomAD v4: 12-6330763-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6330763G>T , CM000674.2:g.6330763G>T	GRCh38
NC_000012.11:g.6439929G>T , CM000674.1:g.6439929G>T	GRCh37
NC_000012.10:g.6310190G>T	NCBI36
NG_007506.1:g.16333C>A , LRG_193:g.16333C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366159.9:n.1727-52C>A
ENST00000437813.8:c.*87-52C>A	ENSP00000513672.1:n.*87-52C>A
ENST00000440083.7:c.845-52C>A	ENSP00000413224.3:n.845-52C>A
ENST00000535038.2:n.808-52C>A
ENST00000535958.2:c.*453-52C>A	ENSP00000513673.1:n.*453-52C>A
ENST00000698337.1:n.564C>A
ENST00000698338.1:n.988C>A
ENST00000698339.1:c.*121-52C>A	ENSP00000513670.1:n.*121-52C>A
ENST00000698340.1:c.552-52C>A	ENSP00000513671.1:n.552-52C>A
ENST00000162749.7:c.626-52C>A MANE Select	ENSP00000162749.2:n.626-52C>A
ENST00000162749.6:c.626-52C>A	ENSP00000162749.2:n.626-52C>A
ENST00000534885.5:c.*103-52C>A	ENSP00000441803.1:n.*103-52C>A
ENST00000535038.1:n.385C>A
ENST00000536717.5:n.530-52C>A
ENST00000537842.5:n.230-52C>A
ENST00000539372.5:c.626-52C>A	ENSP00000442059.1:n.626-52C>A
ENST00000540022.5:c.497-52C>A	ENSP00000438343.1:n.497-52C>A
ENST00000543359.5:n.38-52C>A
ENST00000543995.5:c.*213-52C>A	ENSP00000442405.1:n.*213-52C>A
NM_001065.3:c.626-52C>A , LRG_193t1:c.626-52C>A	NP_001056.1:n.626-52C>A
NM_001346091.1:c.302-52C>A	NP_001333020.1:n.302-52C>A
NM_001346092.1:c.167-52C>A	NP_001333021.1:n.167-52C>A
NR_144351.1:n.855-52C>A
NM_001065.4:c.626-52C>A MANE Select	NP_001056.1:n.626-52C>A
NM_001346091.2:c.302-52C>A	NP_001333020.1:n.302-52C>A
NM_001346092.2:c.167-52C>A	NP_001333021.1:n.167-52C>A
NR_144351.2:n.814-52C>A