Canonical Allele Identifier: CA478504967

Gene: TNFRSF1A

Linked Data

• MyVariant Identifiers: chr12:g.6442567G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6333401G>A , CM000674.2:g.6333401G>A	GRCh38
NC_000012.11:g.6442567G>A , CM000674.1:g.6442567G>A	GRCh37
NC_000012.10:g.6312828G>A	NCBI36
NG_007506.1:g.13695C>T , LRG_193:g.13695C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366159.9:n.472C>T
ENST00000437813.8:c.438C>T	ENSP00000513672.1:p.Cys146=
ENST00000440083.7:c.438C>T	ENSP00000413224.3:p.Cys146=
ENST00000535958.2:c.*265C>T	ENSP00000513673.1:n.*265C>T
ENST00000698339.1:c.438C>T	ENSP00000513670.1:p.Cys146=
ENST00000698340.1:c.438C>T	ENSP00000513671.1:p.Cys146=
ENST00000162749.7:c.438C>T MANE Select	ENSP00000162749.2:p.Cys146=
ENST00000162749.6:c.438C>T	ENSP00000162749.2:p.Cys146=
ENST00000366159.8:c.438C>T	ENSP00000380389.3:p.Cys146=
ENST00000437813.7:n.399C>T
ENST00000440083.6:c.438C>T	ENSP00000413224.2:p.Cys146=
ENST00000534885.5:c.284C>T	ENSP00000441803.1:p.Ala95Val
ENST00000537842.5:n.42C>T
ENST00000539372.5:c.438C>T	ENSP00000442059.1:p.Cys146=
ENST00000540022.5:c.309C>T	ENSP00000438343.1:p.Cys103=
ENST00000543048.5:c.*49C>T	ENSP00000439981.1:n.*49C>T
ENST00000543995.5:c.*25C>T	ENSP00000442405.1:n.*25C>T
NM_001065.3:c.438C>T , LRG_193t1:c.438C>T	NP_001056.1:p.Cys146=
NM_001346091.1:c.114C>T	NP_001333020.1:p.Cys38=
NM_001346092.1:c.-140C>T	NP_001333021.1:n.-140C>T
NR_144351.1:n.741C>T
NM_001065.4:c.438C>T MANE Select	NP_001056.1:p.Cys146=
NM_001346091.2:c.114C>T	NP_001333020.1:p.Cys38=
NM_001346092.2:c.-140C>T	NP_001333021.1:n.-140C>T
NR_144351.2:n.700C>T