Canonical Allele Identifier: CA383547534

Gene: TNFRSF1A

Linked Data

• MyVariant Identifiers: chr12:g.6439786C>T (hg19) ; chr12:g.6330620C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6330620C>T , CM000674.2:g.6330620C>T	GRCh38
NC_000012.11:g.6439786C>T , CM000674.1:g.6439786C>T	GRCh37
NC_000012.10:g.6310047C>T	NCBI36
NG_007506.1:g.16476G>A , LRG_193:g.16476G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366159.9:n.1818G>A
ENST00000437813.8:c.*178G>A	ENSP00000513672.1:n.*178G>A
ENST00000440083.7:c.936G>A	ENSP00000413224.3:p.Trp312Ter
ENST00000535038.2:n.899G>A
ENST00000535958.2:c.*544G>A	ENSP00000513673.1:n.*544G>A
ENST00000698337.1:n.707G>A
ENST00000698338.1:n.1131G>A
ENST00000698339.1:c.*212G>A	ENSP00000513670.1:n.*212G>A
ENST00000698340.1:c.643G>A	ENSP00000513671.1:p.Glu215Lys
ENST00000162749.7:c.717G>A MANE Select	ENSP00000162749.2:p.Trp239Ter
ENST00000162749.6:c.717G>A	ENSP00000162749.2:p.Trp239Ter
ENST00000534885.5:c.*194G>A	ENSP00000441803.1:n.*194G>A
ENST00000535038.1:n.528G>A
ENST00000536717.5:n.621G>A
ENST00000537842.5:n.321G>A
ENST00000539372.5:c.717G>A	ENSP00000442059.1:p.Trp239Ter
ENST00000540022.5:c.588G>A	ENSP00000438343.1:p.Trp196Ter
ENST00000543359.5:n.129G>A
ENST00000543995.5:c.*304G>A	ENSP00000442405.1:n.*304G>A
NM_001065.3:c.717G>A , LRG_193t1:c.717G>A	NP_001056.1:p.Trp239Ter
NM_001346091.1:c.393G>A	NP_001333020.1:p.Trp131Ter
NM_001346092.1:c.258G>A	NP_001333021.1:p.Trp86Ter
NR_144351.1:n.946G>A
NM_001065.4:c.717G>A MANE Select	NP_001056.1:p.Trp239Ter
NM_001346091.2:c.393G>A	NP_001333020.1:p.Trp131Ter
NM_001346092.2:c.258G>A	NP_001333021.1:p.Trp86Ter
NR_144351.2:n.905G>A