Canonical Allele Identifier: CA2617251020

Gene: TNFRSF1A

Linked Data

• gnomAD v4: 12-6330844-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6330844T>G , CM000674.2:g.6330844T>G	GRCh38
NC_000012.11:g.6440010T>G , CM000674.1:g.6440010T>G	GRCh37
NC_000012.10:g.6310271T>G	NCBI36
NG_007506.1:g.16252A>C , LRG_193:g.16252A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366159.9:n.1726+9A>C
ENST00000437813.8:c.*86+9A>C	ENSP00000513672.1:n.*86+9A>C
ENST00000440083.7:c.844+9A>C	ENSP00000413224.3:n.844+9A>C
ENST00000535038.2:n.807+9A>C
ENST00000535958.2:c.*452+9A>C	ENSP00000513673.1:n.*452+9A>C
ENST00000698337.1:n.483A>C
ENST00000698338.1:n.907A>C
ENST00000698339.1:c.*120+9A>C	ENSP00000513670.1:n.*120+9A>C
ENST00000698340.1:c.552-133A>C	ENSP00000513671.1:n.552-133A>C
ENST00000162749.7:c.625+9A>C MANE Select	ENSP00000162749.2:n.625+9A>C
ENST00000162749.6:c.625+9A>C	ENSP00000162749.2:n.625+9A>C
ENST00000534885.5:c.*102+9A>C	ENSP00000441803.1:n.*102+9A>C
ENST00000535038.1:n.304A>C
ENST00000536717.5:n.529+9A>C
ENST00000537842.5:n.229+9A>C
ENST00000539372.5:c.625+9A>C	ENSP00000442059.1:n.625+9A>C
ENST00000540022.5:c.496+9A>C	ENSP00000438343.1:n.496+9A>C
ENST00000543359.5:n.38-133A>C
ENST00000543995.5:c.*212+9A>C	ENSP00000442405.1:n.*212+9A>C
NM_001065.3:c.625+9A>C , LRG_193t1:c.625+9A>C	NP_001056.1:n.625+9A>C
NM_001346091.1:c.301+9A>C	NP_001333020.1:n.301+9A>C
NM_001346092.1:c.166+9A>C	NP_001333021.1:n.166+9A>C
NR_144351.1:n.855-133A>C
NM_001065.4:c.625+9A>C MANE Select	NP_001056.1:n.625+9A>C
NM_001346091.2:c.301+9A>C	NP_001333020.1:n.301+9A>C
NM_001346092.2:c.166+9A>C	NP_001333021.1:n.166+9A>C
NR_144351.2:n.814-133A>C