Canonical Allele Identifier: CA478504802

Gene: TNFRSF1A

Linked Data

• MyVariant Identifiers: chr12:g.6439086G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6329920G>T , CM000674.2:g.6329920G>T	GRCh38
NC_000012.11:g.6439086G>T , CM000674.1:g.6439086G>T	GRCh37
NC_000012.10:g.6309347G>T	NCBI36
NG_007506.1:g.17176C>A , LRG_193:g.17176C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366159.9:n.2016C>A
ENST00000437813.8:c.*376C>A	ENSP00000513672.1:n.*376C>A
ENST00000440083.7:c.1134C>A	ENSP00000413224.3:p.Pro378=
ENST00000535958.2:c.*742C>A	ENSP00000513673.1:n.*742C>A
ENST00000698337.1:n.876C>A
ENST00000698338.1:n.1529C>A
ENST00000698339.1:c.*410C>A	ENSP00000513670.1:n.*410C>A
ENST00000698340.1:c.*154C>A	ENSP00000513671.1:n.*154C>A
ENST00000162749.7:c.915C>A MANE Select	ENSP00000162749.2:p.Pro305=
ENST00000162749.6:c.915C>A	ENSP00000162749.2:p.Pro305=
ENST00000534885.5:c.*392C>A	ENSP00000441803.1:n.*392C>A
ENST00000536717.5:n.819C>A
ENST00000537842.5:n.373-21C>A
ENST00000540022.5:c.786C>A	ENSP00000438343.1:p.Pro262=
ENST00000543359.5:n.327C>A
ENST00000543995.5:c.*502C>A	ENSP00000442405.1:n.*502C>A
NM_001065.3:c.915C>A , LRG_193t1:c.915C>A	NP_001056.1:p.Pro305=
NM_001346091.1:c.591C>A	NP_001333020.1:p.Pro197=
NM_001346092.1:c.456C>A	NP_001333021.1:p.Pro152=
NR_144351.1:n.1144C>A
NM_001065.4:c.915C>A MANE Select	NP_001056.1:p.Pro305=
NM_001346091.2:c.591C>A	NP_001333020.1:p.Pro197=
NM_001346092.2:c.456C>A	NP_001333021.1:p.Pro152=
NR_144351.2:n.1103C>A