Canonical Allele Identifier: CA383545889

Gene: TNFRSF1A

Linked Data

• MyVariant Identifiers: chr12:g.6439082A>T (hg19) ; chr12:g.6329916A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6329916A>T , CM000674.2:g.6329916A>T	GRCh38
NC_000012.11:g.6439082A>T , CM000674.1:g.6439082A>T	GRCh37
NC_000012.10:g.6309343A>T	NCBI36
NG_007506.1:g.17180T>A , LRG_193:g.17180T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366159.9:n.2020T>A
ENST00000437813.8:c.*380T>A	ENSP00000513672.1:n.*380T>A
ENST00000440083.7:c.1138T>A	ENSP00000413224.3:p.Phe380Ile
ENST00000535958.2:c.*746T>A	ENSP00000513673.1:n.*746T>A
ENST00000698337.1:n.880T>A
ENST00000698338.1:n.1533T>A
ENST00000698339.1:c.*414T>A	ENSP00000513670.1:n.*414T>A
ENST00000698340.1:c.*158T>A	ENSP00000513671.1:n.*158T>A
ENST00000162749.7:c.919T>A MANE Select	ENSP00000162749.2:p.Phe307Ile
ENST00000162749.6:c.919T>A	ENSP00000162749.2:p.Phe307Ile
ENST00000534885.5:c.*396T>A	ENSP00000441803.1:n.*396T>A
ENST00000536717.5:n.823T>A
ENST00000537842.5:n.373-17T>A
ENST00000540022.5:c.790T>A	ENSP00000438343.1:p.Phe264Ile
ENST00000543359.5:n.331T>A
ENST00000543995.5:c.*506T>A	ENSP00000442405.1:n.*506T>A
NM_001065.3:c.919T>A , LRG_193t1:c.919T>A	NP_001056.1:p.Phe307Ile
NM_001346091.1:c.595T>A	NP_001333020.1:p.Phe199Ile
NM_001346092.1:c.460T>A	NP_001333021.1:p.Phe154Ile
NR_144351.1:n.1148T>A
NM_001065.4:c.919T>A MANE Select	NP_001056.1:p.Phe307Ile
NM_001346091.2:c.595T>A	NP_001333020.1:p.Phe199Ile
NM_001346092.2:c.460T>A	NP_001333021.1:p.Phe154Ile
NR_144351.2:n.1107T>A