Canonical Allele Identifier: CA383550620

Gene: TNFRSF1A

Linked Data

• MyVariant Identifiers: chr12:g.6442980C>T (hg19) ; chr12:g.6333814C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6333814C>T , CM000674.2:g.6333814C>T	GRCh38
NC_000012.11:g.6442980C>T , CM000674.1:g.6442980C>T	GRCh37
NC_000012.10:g.6313241C>T	NCBI36
NG_007506.1:g.13282G>A , LRG_193:g.13282G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366159.9:n.279G>A
ENST00000437813.8:c.245G>A	ENSP00000513672.1:p.Arg82Lys
ENST00000440083.7:c.245G>A	ENSP00000413224.3:p.Arg82Lys
ENST00000535958.2:c.*72G>A	ENSP00000513673.1:n.*72G>A
ENST00000698339.1:c.245G>A	ENSP00000513670.1:p.Arg82Lys
ENST00000698340.1:c.245G>A	ENSP00000513671.1:p.Arg82Lys
ENST00000162749.7:c.245G>A MANE Select	ENSP00000162749.2:p.Arg82Lys
ENST00000162749.6:c.245G>A	ENSP00000162749.2:p.Arg82Lys
ENST00000366159.8:c.245G>A	ENSP00000380389.3:p.Arg82Lys
ENST00000437813.7:n.206G>A
ENST00000440083.6:c.245G>A	ENSP00000413224.2:p.Arg82Lys
ENST00000534885.5:c.91G>A	ENSP00000441803.1:p.Gly31Arg
ENST00000535958.1:n.491G>A
ENST00000536194.1:c.218G>A	ENSP00000442919.1:p.Arg73Lys
ENST00000539372.5:c.245G>A	ENSP00000442059.1:p.Arg82Lys
ENST00000540022.5:c.193+277G>A	ENSP00000438343.1:n.193+277G>A
ENST00000543048.5:c.214+31G>A	ENSP00000439981.1:n.214+31G>A
ENST00000543995.5:c.193+277G>A	ENSP00000442405.1:n.193+277G>A
NM_001065.3:c.245G>A , LRG_193t1:c.245G>A	NP_001056.1:p.Arg82Lys
NM_001346091.1:c.-80G>A	NP_001333020.1:n.-80G>A
NM_001346092.1:c.-333G>A	NP_001333021.1:n.-333G>A
NR_144351.1:n.548G>A
NM_001065.4:c.245G>A MANE Select	NP_001056.1:p.Arg82Lys
NM_001346091.2:c.-80G>A	NP_001333020.1:n.-80G>A
NM_001346092.2:c.-333G>A	NP_001333021.1:n.-333G>A
NR_144351.2:n.507G>A