Canonical Allele Identifier: CA383545885

Gene: TNFRSF1A

Linked Data

• MyVariant Identifiers: chr12:g.6439081A>T (hg19) ; chr12:g.6329915A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6329915A>T , CM000674.2:g.6329915A>T	GRCh38
NC_000012.11:g.6439081A>T , CM000674.1:g.6439081A>T	GRCh37
NC_000012.10:g.6309342A>T	NCBI36
NG_007506.1:g.17181T>A , LRG_193:g.17181T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000366159.9:n.2021T>A
ENST00000437813.8:c.*381T>A	ENSP00000513672.1:n.*381T>A
ENST00000440083.7:c.1139T>A	ENSP00000413224.3:p.Phe380Tyr
ENST00000535958.2:c.*747T>A	ENSP00000513673.1:n.*747T>A
ENST00000698337.1:n.881T>A
ENST00000698338.1:n.1534T>A
ENST00000698339.1:c.*415T>A	ENSP00000513670.1:n.*415T>A
ENST00000698340.1:c.*159T>A	ENSP00000513671.1:n.*159T>A
ENST00000162749.7:c.920T>A MANE Select	ENSP00000162749.2:p.Phe307Tyr
ENST00000162749.6:c.920T>A	ENSP00000162749.2:p.Phe307Tyr
ENST00000534885.5:c.*397T>A	ENSP00000441803.1:n.*397T>A
ENST00000536717.5:n.824T>A
ENST00000537842.5:n.373-16T>A
ENST00000540022.5:c.791T>A	ENSP00000438343.1:p.Phe264Tyr
ENST00000543359.5:n.332T>A
ENST00000543995.5:c.*507T>A	ENSP00000442405.1:n.*507T>A
NM_001065.3:c.920T>A , LRG_193t1:c.920T>A	NP_001056.1:p.Phe307Tyr
NM_001346091.1:c.596T>A	NP_001333020.1:p.Phe199Tyr
NM_001346092.1:c.461T>A	NP_001333021.1:p.Phe154Tyr
NR_144351.1:n.1149T>A
NM_001065.4:c.920T>A MANE Select	NP_001056.1:p.Phe307Tyr
NM_001346091.2:c.596T>A	NP_001333020.1:p.Phe199Tyr
NM_001346092.2:c.461T>A	NP_001333021.1:p.Phe154Tyr
NR_144351.2:n.1108T>A