Canonical Allele Identifier: CA690827667

Gene: TNFRSF1A

Linked Data

• dbSNP Id: rs1228878027
• MyVariant Identifiers: chr12:g.6440002A>T (hg19) ; chr12:g.6330836A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6330836A>T , CM000674.2:g.6330836A>T	GRCh38
NC_000012.11:g.6440002A>T , CM000674.1:g.6440002A>T	GRCh37
NC_000012.10:g.6310263A>T	NCBI36
NG_007506.1:g.16260T>A , LRG_193:g.16260T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366159.9:n.1726+17T>A
ENST00000437813.8:c.*86+17T>A	ENSP00000513672.1:n.*86+17T>A
ENST00000440083.7:c.844+17T>A	ENSP00000413224.3:n.844+17T>A
ENST00000535038.2:n.807+17T>A
ENST00000535958.2:c.*452+17T>A	ENSP00000513673.1:n.*452+17T>A
ENST00000698337.1:n.491T>A
ENST00000698338.1:n.915T>A
ENST00000698339.1:c.*120+17T>A	ENSP00000513670.1:n.*120+17T>A
ENST00000698340.1:c.552-125T>A	ENSP00000513671.1:n.552-125T>A
ENST00000162749.7:c.625+17T>A MANE Select	ENSP00000162749.2:n.625+17T>A
ENST00000162749.6:c.625+17T>A	ENSP00000162749.2:n.625+17T>A
ENST00000534885.5:c.*102+17T>A	ENSP00000441803.1:n.*102+17T>A
ENST00000535038.1:n.312T>A
ENST00000536717.5:n.529+17T>A
ENST00000537842.5:n.229+17T>A
ENST00000539372.5:c.625+17T>A	ENSP00000442059.1:n.625+17T>A
ENST00000540022.5:c.496+17T>A	ENSP00000438343.1:n.496+17T>A
ENST00000543359.5:n.38-125T>A
ENST00000543995.5:c.*212+17T>A	ENSP00000442405.1:n.*212+17T>A
NM_001065.3:c.625+17T>A , LRG_193t1:c.625+17T>A	NP_001056.1:n.625+17T>A
NM_001346091.1:c.301+17T>A	NP_001333020.1:n.301+17T>A
NM_001346092.1:c.166+17T>A	NP_001333021.1:n.166+17T>A
NR_144351.1:n.855-125T>A
NM_001065.4:c.625+17T>A MANE Select	NP_001056.1:n.625+17T>A
NM_001346091.2:c.301+17T>A	NP_001333020.1:n.301+17T>A
NM_001346092.2:c.166+17T>A	NP_001333021.1:n.166+17T>A
NR_144351.2:n.814-125T>A