Canonical Allele Identifier: CA383547764

Gene: TNFRSF1A

Linked Data

• MyVariant Identifiers: chr12:g.6439845A>G (hg19) ; chr12:g.6330679A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6330679A>G , CM000674.2:g.6330679A>G	GRCh38
NC_000012.11:g.6439845A>G , CM000674.1:g.6439845A>G	GRCh37
NC_000012.10:g.6310106A>G	NCBI36
NG_007506.1:g.16417T>C , LRG_193:g.16417T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366159.9:n.1759T>C
ENST00000437813.8:c.*119T>C	ENSP00000513672.1:n.*119T>C
ENST00000440083.7:c.877T>C	ENSP00000413224.3:p.Phe293Leu
ENST00000535038.2:n.840T>C
ENST00000535958.2:c.*485T>C	ENSP00000513673.1:n.*485T>C
ENST00000698337.1:n.648T>C
ENST00000698338.1:n.1072T>C
ENST00000698339.1:c.*153T>C	ENSP00000513670.1:n.*153T>C
ENST00000698340.1:c.584T>C	ENSP00000513671.1:p.Leu195Pro
ENST00000162749.7:c.658T>C MANE Select	ENSP00000162749.2:p.Phe220Leu
ENST00000162749.6:c.658T>C	ENSP00000162749.2:p.Phe220Leu
ENST00000534885.5:c.*135T>C	ENSP00000441803.1:n.*135T>C
ENST00000535038.1:n.469T>C
ENST00000536717.5:n.562T>C
ENST00000537842.5:n.262T>C
ENST00000539372.5:c.658T>C	ENSP00000442059.1:p.Phe220Leu
ENST00000540022.5:c.529T>C	ENSP00000438343.1:p.Phe177Leu
ENST00000543359.5:n.70T>C
ENST00000543995.5:c.*245T>C	ENSP00000442405.1:n.*245T>C
NM_001065.3:c.658T>C , LRG_193t1:c.658T>C	NP_001056.1:p.Phe220Leu
NM_001346091.1:c.334T>C	NP_001333020.1:p.Phe112Leu
NM_001346092.1:c.199T>C	NP_001333021.1:p.Phe67Leu
NR_144351.1:n.887T>C
NM_001065.4:c.658T>C MANE Select	NP_001056.1:p.Phe220Leu
NM_001346091.2:c.334T>C	NP_001333020.1:p.Phe112Leu
NM_001346092.2:c.199T>C	NP_001333021.1:p.Phe67Leu
NR_144351.2:n.846T>C