Canonical Allele Identifier: CA383547753

Gene: TNFRSF1A

Linked Data

• MyVariant Identifiers: chr12:g.6439843A>C (hg19) ; chr12:g.6330677A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6330677A>C , CM000674.2:g.6330677A>C	GRCh38
NC_000012.11:g.6439843A>C , CM000674.1:g.6439843A>C	GRCh37
NC_000012.10:g.6310104A>C	NCBI36
NG_007506.1:g.16419T>G , LRG_193:g.16419T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366159.9:n.1761T>G
ENST00000437813.8:c.*121T>G	ENSP00000513672.1:n.*121T>G
ENST00000440083.7:c.879T>G	ENSP00000413224.3:p.Phe293Leu
ENST00000535038.2:n.842T>G
ENST00000535958.2:c.*487T>G	ENSP00000513673.1:n.*487T>G
ENST00000698337.1:n.650T>G
ENST00000698338.1:n.1074T>G
ENST00000698339.1:c.*155T>G	ENSP00000513670.1:n.*155T>G
ENST00000698340.1:c.586T>G	ENSP00000513671.1:p.Trp196Gly
ENST00000162749.7:c.660T>G MANE Select	ENSP00000162749.2:p.Phe220Leu
ENST00000162749.6:c.660T>G	ENSP00000162749.2:p.Phe220Leu
ENST00000534885.5:c.*137T>G	ENSP00000441803.1:n.*137T>G
ENST00000535038.1:n.471T>G
ENST00000536717.5:n.564T>G
ENST00000537842.5:n.264T>G
ENST00000539372.5:c.660T>G	ENSP00000442059.1:p.Phe220Leu
ENST00000540022.5:c.531T>G	ENSP00000438343.1:p.Phe177Leu
ENST00000543359.5:n.72T>G
ENST00000543995.5:c.*247T>G	ENSP00000442405.1:n.*247T>G
NM_001065.3:c.660T>G , LRG_193t1:c.660T>G	NP_001056.1:p.Phe220Leu
NM_001346091.1:c.336T>G	NP_001333020.1:p.Phe112Leu
NM_001346092.1:c.201T>G	NP_001333021.1:p.Phe67Leu
NR_144351.1:n.889T>G
NM_001065.4:c.660T>G MANE Select	NP_001056.1:p.Phe220Leu
NM_001346091.2:c.336T>G	NP_001333020.1:p.Phe112Leu
NM_001346092.2:c.201T>G	NP_001333021.1:p.Phe67Leu
NR_144351.2:n.848T>G