Canonical Allele Identifier: CA280815

Gene: TNFRSF1A

Linked Data

• ClinVar Variation Id: 97686
• ClinVar RCV Id: RCV000083939 ; RCV000214793
• dbSNP Id: rs104895228
• MyVariant Identifiers: chr12:g.6442930A>G (hg19) ; chr12:g.6333764A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6333764A>G , CM000674.2:g.6333764A>G	GRCh38
NC_000012.11:g.6442930A>G , CM000674.1:g.6442930A>G	GRCh37
NC_000012.10:g.6313191A>G	NCBI36
NG_007506.1:g.13332T>C , LRG_193:g.13332T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366159.9:n.329T>C
ENST00000437813.8:c.295T>C	ENSP00000513672.1:p.Cys99Arg
ENST00000440083.7:c.295T>C	ENSP00000413224.3:p.Cys99Arg
ENST00000535958.2:c.*122T>C	ENSP00000513673.1:n.*122T>C
ENST00000698339.1:c.295T>C	ENSP00000513670.1:p.Cys99Arg
ENST00000698340.1:c.295T>C	ENSP00000513671.1:p.Cys99Arg
ENST00000162749.7:c.295T>C MANE Select	ENSP00000162749.2:p.Cys99Arg
ENST00000162749.6:c.295T>C	ENSP00000162749.2:p.Cys99Arg
ENST00000366159.8:c.295T>C	ENSP00000380389.3:p.Cys99Arg
ENST00000437813.7:n.256T>C
ENST00000440083.6:c.295T>C	ENSP00000413224.2:p.Cys99Arg
ENST00000534885.5:c.141T>C	ENSP00000441803.1:p.Thr47=
ENST00000535958.1:n.541T>C
ENST00000536194.1:c.268T>C	ENSP00000442919.1:p.Cys90Arg
ENST00000539372.5:c.295T>C	ENSP00000442059.1:p.Cys99Arg
ENST00000540022.5:c.194-248T>C	ENSP00000438343.1:n.194-248T>C
ENST00000543048.5:c.214+81T>C	ENSP00000439981.1:n.214+81T>C
ENST00000543995.5:c.194-313T>C	ENSP00000442405.1:n.194-313T>C
NM_001065.3:c.295T>C , LRG_193t1:c.295T>C	NP_001056.1:p.Cys99Arg
NM_001346091.1:c.-30T>C	NP_001333020.1:n.-30T>C
NM_001346092.1:c.-283T>C	NP_001333021.1:n.-283T>C
NR_144351.1:n.598T>C
NM_001065.4:c.295T>C MANE Select	NP_001056.1:p.Cys99Arg
NM_001346091.2:c.-30T>C	NP_001333020.1:n.-30T>C
NM_001346092.2:c.-283T>C	NP_001333021.1:n.-283T>C
NR_144351.2:n.557T>C