Canonical Allele Identifier: CA478504745

Gene: TNFRSF1A

Linked Data

• MyVariant Identifiers: chr12:g.6438966G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6329800G>T , CM000674.2:g.6329800G>T	GRCh38
NC_000012.11:g.6438966G>T , CM000674.1:g.6438966G>T	GRCh37
NC_000012.10:g.6309227G>T	NCBI36
NG_007506.1:g.17296C>A , LRG_193:g.17296C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000366159.9:n.2136C>A
ENST00000437813.8:c.*496C>A	ENSP00000513672.1:n.*496C>A
ENST00000440083.7:c.1254C>A	ENSP00000413224.3:p.Ala418=
ENST00000535958.2:c.*862C>A	ENSP00000513673.1:n.*862C>A
ENST00000698337.1:n.996C>A
ENST00000698338.1:n.1649C>A
ENST00000698339.1:c.*530C>A	ENSP00000513670.1:n.*530C>A
ENST00000698340.1:c.*274C>A	ENSP00000513671.1:n.*274C>A
ENST00000162749.7:c.1035C>A MANE Select	ENSP00000162749.2:p.Ala345=
ENST00000162749.6:c.1035C>A	ENSP00000162749.2:p.Ala345=
ENST00000534885.5:c.*512C>A	ENSP00000441803.1:n.*512C>A
ENST00000536717.5:n.939C>A
ENST00000540022.5:c.906C>A	ENSP00000438343.1:p.Ala302=
ENST00000543359.5:n.447C>A
ENST00000543995.5:c.*622C>A	ENSP00000442405.1:n.*622C>A
NM_001065.3:c.1035C>A , LRG_193t1:c.1035C>A	NP_001056.1:p.Ala345=
NM_001346091.1:c.711C>A	NP_001333020.1:p.Ala237=
NM_001346092.1:c.576C>A	NP_001333021.1:p.Ala192=
NR_144351.1:n.1264C>A
NM_001065.4:c.1035C>A MANE Select	NP_001056.1:p.Ala345=
NM_001346091.2:c.711C>A	NP_001333020.1:p.Ala237=
NM_001346092.2:c.576C>A	NP_001333021.1:p.Ala192=
NR_144351.2:n.1223C>A