Canonical Allele Identifier: CA383547681

Gene: TNFRSF1A

Linked Data

• MyVariant Identifiers: chr12:g.6439826G>T (hg19) ; chr12:g.6330660G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6330660G>T , CM000674.2:g.6330660G>T	GRCh38
NC_000012.11:g.6439826G>T , CM000674.1:g.6439826G>T	GRCh37
NC_000012.10:g.6310087G>T	NCBI36
NG_007506.1:g.16436C>A , LRG_193:g.16436C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366159.9:n.1778C>A
ENST00000437813.8:c.*138C>A	ENSP00000513672.1:n.*138C>A
ENST00000440083.7:c.896C>A	ENSP00000413224.3:p.Ser299Tyr
ENST00000535038.2:n.859C>A
ENST00000535958.2:c.*504C>A	ENSP00000513673.1:n.*504C>A
ENST00000698337.1:n.667C>A
ENST00000698338.1:n.1091C>A
ENST00000698339.1:c.*172C>A	ENSP00000513670.1:n.*172C>A
ENST00000698340.1:c.603C>A	ENSP00000513671.1:p.Ile201=
ENST00000162749.7:c.677C>A MANE Select	ENSP00000162749.2:p.Ser226Tyr
ENST00000162749.6:c.677C>A	ENSP00000162749.2:p.Ser226Tyr
ENST00000534885.5:c.*154C>A	ENSP00000441803.1:n.*154C>A
ENST00000535038.1:n.488C>A
ENST00000536717.5:n.581C>A
ENST00000537842.5:n.281C>A
ENST00000539372.5:c.677C>A	ENSP00000442059.1:p.Ser226Tyr
ENST00000540022.5:c.548C>A	ENSP00000438343.1:p.Ser183Tyr
ENST00000543359.5:n.89C>A
ENST00000543995.5:c.*264C>A	ENSP00000442405.1:n.*264C>A
NM_001065.3:c.677C>A , LRG_193t1:c.677C>A	NP_001056.1:p.Ser226Tyr
NM_001346091.1:c.353C>A	NP_001333020.1:p.Ser118Tyr
NM_001346092.1:c.218C>A	NP_001333021.1:p.Ser73Tyr
NR_144351.1:n.906C>A
NM_001065.4:c.677C>A MANE Select	NP_001056.1:p.Ser226Tyr
NM_001346091.2:c.353C>A	NP_001333020.1:p.Ser118Tyr
NM_001346092.2:c.218C>A	NP_001333021.1:p.Ser73Tyr
NR_144351.2:n.865C>A