Canonical Allele Identifier: CA478504799

Gene: TNFRSF1A

Linked Data

• MyVariant Identifiers: chr12:g.6439080A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6329914A>G , CM000674.2:g.6329914A>G	GRCh38
NC_000012.11:g.6439080A>G , CM000674.1:g.6439080A>G	GRCh37
NC_000012.10:g.6309341A>G	NCBI36
NG_007506.1:g.17182T>C , LRG_193:g.17182T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366159.9:n.2022T>C
ENST00000437813.8:c.*382T>C	ENSP00000513672.1:n.*382T>C
ENST00000440083.7:c.1140T>C	ENSP00000413224.3:p.Phe380=
ENST00000535958.2:c.*748T>C	ENSP00000513673.1:n.*748T>C
ENST00000698337.1:n.882T>C
ENST00000698338.1:n.1535T>C
ENST00000698339.1:c.*416T>C	ENSP00000513670.1:n.*416T>C
ENST00000698340.1:c.*160T>C	ENSP00000513671.1:n.*160T>C
ENST00000162749.7:c.921T>C MANE Select	ENSP00000162749.2:p.Phe307=
ENST00000162749.6:c.921T>C	ENSP00000162749.2:p.Phe307=
ENST00000534885.5:c.*398T>C	ENSP00000441803.1:n.*398T>C
ENST00000536717.5:n.825T>C
ENST00000537842.5:n.373-15T>C
ENST00000540022.5:c.792T>C	ENSP00000438343.1:p.Phe264=
ENST00000543359.5:n.333T>C
ENST00000543995.5:c.*508T>C	ENSP00000442405.1:n.*508T>C
NM_001065.3:c.921T>C , LRG_193t1:c.921T>C	NP_001056.1:p.Phe307=
NM_001346091.1:c.597T>C	NP_001333020.1:p.Phe199=
NM_001346092.1:c.462T>C	NP_001333021.1:p.Phe154=
NR_144351.1:n.1150T>C
NM_001065.4:c.921T>C MANE Select	NP_001056.1:p.Phe307=
NM_001346091.2:c.597T>C	NP_001333020.1:p.Phe199=
NM_001346092.2:c.462T>C	NP_001333021.1:p.Phe154=
NR_144351.2:n.1109T>C