Canonical Allele Identifier: CA280751

Gene: TNFRSF1A

Linked Data

• ClinVar Variation Id: 97664
• ClinVar RCV Id: RCV000083917
• dbSNP Id: rs104895252
• MyVariant Identifiers: chr12:g.6443010C>T (hg19) ; chr12:g.6333844C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6333844C>T , CM000674.2:g.6333844C>T	GRCh38
NC_000012.11:g.6443010C>T , CM000674.1:g.6443010C>T	GRCh37
NC_000012.10:g.6313271C>T	NCBI36
NG_007506.1:g.13252G>A , LRG_193:g.13252G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366159.9:n.249G>A
ENST00000437813.8:c.215G>A	ENSP00000513672.1:p.Cys72Tyr
ENST00000440083.7:c.215G>A	ENSP00000413224.3:p.Cys72Tyr
ENST00000535958.2:c.*42G>A	ENSP00000513673.1:n.*42G>A
ENST00000698339.1:c.215G>A	ENSP00000513670.1:p.Cys72Tyr
ENST00000698340.1:c.215G>A	ENSP00000513671.1:p.Cys72Tyr
ENST00000162749.7:c.215G>A MANE Select	ENSP00000162749.2:p.Cys72Tyr
ENST00000162749.6:c.215G>A	ENSP00000162749.2:p.Cys72Tyr
ENST00000366159.8:c.215G>A	ENSP00000380389.3:p.Cys72Tyr
ENST00000437813.7:n.176G>A
ENST00000440083.6:c.215G>A	ENSP00000413224.2:p.Cys72Tyr
ENST00000534885.5:c.61G>A	ENSP00000441803.1:p.Val21Ile
ENST00000535958.1:n.461G>A
ENST00000536194.1:c.194-6G>A	ENSP00000442919.1:n.194-6G>A
ENST00000539372.5:c.215G>A	ENSP00000442059.1:p.Cys72Tyr
ENST00000540022.5:c.193+247G>A	ENSP00000438343.1:n.193+247G>A
ENST00000543048.5:c.214+1G>A	ENSP00000439981.1:n.214+1G>A
ENST00000543995.5:c.193+247G>A	ENSP00000442405.1:n.193+247G>A
NM_001065.3:c.215G>A , LRG_193t1:c.215G>A	NP_001056.1:p.Cys72Tyr
NM_001346091.1:c.-110G>A	NP_001333020.1:n.-110G>A
NM_001346092.1:c.-363G>A	NP_001333021.1:n.-363G>A
NR_144351.1:n.518G>A
NM_001065.4:c.215G>A MANE Select	NP_001056.1:p.Cys72Tyr
NM_001346091.2:c.-110G>A	NP_001333020.1:n.-110G>A
NM_001346092.2:c.-363G>A	NP_001333021.1:n.-363G>A
NR_144351.2:n.477G>A