Canonical Allele Identifier: CA478112805

Gene: TNFRSF1A

Linked Data

• MyVariant Identifiers: chr12:g.6440053G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6330887G>T , CM000674.2:g.6330887G>T	GRCh38
NC_000012.11:g.6440053G>T , CM000674.1:g.6440053G>T	GRCh37
NC_000012.10:g.6310314G>T	NCBI36
NG_007506.1:g.16209C>A , LRG_193:g.16209C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366159.9:n.1692C>A
ENST00000437813.8:c.*52C>A	ENSP00000513672.1:n.*52C>A
ENST00000440083.7:c.810C>A	ENSP00000413224.3:p.Pro270=
ENST00000535038.2:n.773C>A
ENST00000535958.2:c.*418C>A	ENSP00000513673.1:n.*418C>A
ENST00000698337.1:n.440C>A
ENST00000698338.1:n.864C>A
ENST00000698339.1:c.*86C>A	ENSP00000513670.1:n.*86C>A
ENST00000698340.1:c.552-176C>A	ENSP00000513671.1:n.552-176C>A
ENST00000162749.7:c.591C>A MANE Select	ENSP00000162749.2:p.Pro197=
ENST00000162749.6:c.591C>A	ENSP00000162749.2:p.Pro197=
ENST00000534885.5:c.*68C>A	ENSP00000441803.1:n.*68C>A
ENST00000535038.1:n.261C>A
ENST00000536717.5:n.495C>A
ENST00000537842.5:n.195C>A
ENST00000539372.5:c.591C>A	ENSP00000442059.1:p.Pro197=
ENST00000540022.5:c.462C>A	ENSP00000438343.1:p.Pro154=
ENST00000543359.5:n.38-176C>A
ENST00000543995.5:c.*178C>A	ENSP00000442405.1:n.*178C>A
NM_001065.3:c.591C>A , LRG_193t1:c.591C>A	NP_001056.1:p.Pro197=
NM_001346091.1:c.267C>A	NP_001333020.1:p.Pro89=
NM_001346092.1:c.132C>A	NP_001333021.1:p.Pro44=
NR_144351.1:n.855-176C>A
NM_001065.4:c.591C>A MANE Select	NP_001056.1:p.Pro197=
NM_001346091.2:c.267C>A	NP_001333020.1:p.Pro89=
NM_001346092.2:c.132C>A	NP_001333021.1:p.Pro44=
NR_144351.2:n.814-176C>A