Canonical Allele Identifier: CA383545614

Gene: TNFRSF1A

Linked Data

• MyVariant Identifiers: chr12:g.6438967G>T (hg19) ; chr12:g.6329801G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6329801G>T , CM000674.2:g.6329801G>T	GRCh38
NC_000012.11:g.6438967G>T , CM000674.1:g.6438967G>T	GRCh37
NC_000012.10:g.6309228G>T	NCBI36
NG_007506.1:g.17295C>A , LRG_193:g.17295C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000366159.9:n.2135C>A
ENST00000437813.8:c.*495C>A	ENSP00000513672.1:n.*495C>A
ENST00000440083.7:c.1253C>A	ENSP00000413224.3:p.Ala418Asp
ENST00000535958.2:c.*861C>A	ENSP00000513673.1:n.*861C>A
ENST00000698337.1:n.995C>A
ENST00000698338.1:n.1648C>A
ENST00000698339.1:c.*529C>A	ENSP00000513670.1:n.*529C>A
ENST00000698340.1:c.*273C>A	ENSP00000513671.1:n.*273C>A
ENST00000162749.7:c.1034C>A MANE Select	ENSP00000162749.2:p.Ala345Asp
ENST00000162749.6:c.1034C>A	ENSP00000162749.2:p.Ala345Asp
ENST00000534885.5:c.*511C>A	ENSP00000441803.1:n.*511C>A
ENST00000536717.5:n.938C>A
ENST00000540022.5:c.905C>A	ENSP00000438343.1:p.Ala302Asp
ENST00000543359.5:n.446C>A
ENST00000543995.5:c.*621C>A	ENSP00000442405.1:n.*621C>A
NM_001065.3:c.1034C>A , LRG_193t1:c.1034C>A	NP_001056.1:p.Ala345Asp
NM_001346091.1:c.710C>A	NP_001333020.1:p.Ala237Asp
NM_001346092.1:c.575C>A	NP_001333021.1:p.Ala192Asp
NR_144351.1:n.1263C>A
NM_001065.4:c.1034C>A MANE Select	NP_001056.1:p.Ala345Asp
NM_001346091.2:c.710C>A	NP_001333020.1:p.Ala237Asp
NM_001346092.2:c.575C>A	NP_001333021.1:p.Ala192Asp
NR_144351.2:n.1222C>A