Canonical Allele Identifier: CA383548084

Gene: TNFRSF1A

Linked Data

• MyVariant Identifiers: chr12:g.6440060C>T (hg19) ; chr12:g.6330894C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6330894C>T , CM000674.2:g.6330894C>T	GRCh38
NC_000012.11:g.6440060C>T , CM000674.1:g.6440060C>T	GRCh37
NC_000012.10:g.6310321C>T	NCBI36
NG_007506.1:g.16202G>A , LRG_193:g.16202G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366159.9:n.1685G>A
ENST00000437813.8:c.*45G>A	ENSP00000513672.1:n.*45G>A
ENST00000440083.7:c.803G>A	ENSP00000413224.3:p.Cys268Tyr
ENST00000535038.2:n.766G>A
ENST00000535958.2:c.*411G>A	ENSP00000513673.1:n.*411G>A
ENST00000698337.1:n.433G>A
ENST00000698338.1:n.857G>A
ENST00000698339.1:c.*79G>A	ENSP00000513670.1:n.*79G>A
ENST00000698340.1:c.552-183G>A	ENSP00000513671.1:n.552-183G>A
ENST00000162749.7:c.584G>A MANE Select	ENSP00000162749.2:p.Cys195Tyr
ENST00000162749.6:c.584G>A	ENSP00000162749.2:p.Cys195Tyr
ENST00000534885.5:c.*61G>A	ENSP00000441803.1:n.*61G>A
ENST00000535038.1:n.254G>A
ENST00000536717.5:n.488G>A
ENST00000537842.5:n.188G>A
ENST00000539372.5:c.584G>A	ENSP00000442059.1:p.Cys195Tyr
ENST00000540022.5:c.455G>A	ENSP00000438343.1:p.Cys152Tyr
ENST00000543359.5:n.38-183G>A
ENST00000543995.5:c.*171G>A	ENSP00000442405.1:n.*171G>A
NM_001065.3:c.584G>A , LRG_193t1:c.584G>A	NP_001056.1:p.Cys195Tyr
NM_001346091.1:c.260G>A	NP_001333020.1:p.Cys87Tyr
NM_001346092.1:c.125G>A	NP_001333021.1:p.Cys42Tyr
NR_144351.1:n.855-183G>A
NM_001065.4:c.584G>A MANE Select	NP_001056.1:p.Cys195Tyr
NM_001346091.2:c.260G>A	NP_001333020.1:p.Cys87Tyr
NM_001346092.2:c.125G>A	NP_001333021.1:p.Cys42Tyr
NR_144351.2:n.814-183G>A