Canonical Allele Identifier: CA280704

Gene: TNFRSF1A

Linked Data

• ClinVar Variation Id: 97646
• ClinVar RCV Id: RCV000083899 ; RCV001701502
• dbSNP Id: rs104895227
• MyVariant Identifiers: chr12:g.6443299G>A (hg19) ; chr12:g.6334133G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6334133G>A , CM000674.2:g.6334133G>A	GRCh38
NC_000012.11:g.6443299G>A , CM000674.1:g.6443299G>A	GRCh37
NC_000012.10:g.6313560G>A	NCBI36
NG_007506.1:g.12963C>T , LRG_193:g.12963C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366159.9:n.185C>T
ENST00000437813.8:c.151C>T	ENSP00000513672.1:p.His51Tyr
ENST00000440083.7:c.151C>T	ENSP00000413224.3:p.His51Tyr
ENST00000535958.2:c.151C>T	ENSP00000513673.1:p.His51Tyr
ENST00000698339.1:c.151C>T	ENSP00000513670.1:p.His51Tyr
ENST00000698340.1:c.151C>T	ENSP00000513671.1:p.His51Tyr
ENST00000162749.7:c.151C>T MANE Select	ENSP00000162749.2:p.His51Tyr
ENST00000162749.6:c.151C>T	ENSP00000162749.2:p.His51Tyr
ENST00000366159.8:c.151C>T	ENSP00000380389.3:p.His51Tyr
ENST00000437813.7:n.112C>T
ENST00000440083.6:c.151C>T	ENSP00000413224.2:p.His51Tyr
ENST00000534885.5:c.40-268C>T	ENSP00000441803.1:n.40-268C>T
ENST00000535958.1:n.372C>T
ENST00000536194.1:c.151C>T	ENSP00000442919.1:p.His51Tyr
ENST00000538363.1:n.341C>T
ENST00000539372.5:c.151C>T	ENSP00000442059.1:p.His51Tyr
ENST00000540022.5:c.151C>T	ENSP00000438343.1:p.His51Tyr
ENST00000543048.5:c.151C>T	ENSP00000439981.1:p.His51Tyr
ENST00000543995.5:c.151C>T	ENSP00000442405.1:p.His51Tyr
NM_001065.3:c.151C>T , LRG_193t1:c.151C>T	NP_001056.1:p.His51Tyr
NM_001346091.1:c.-131-268C>T	NP_001333020.1:n.-131-268C>T
NM_001346092.1:c.-427C>T	NP_001333021.1:n.-427C>T
NR_144351.1:n.454C>T
NM_001065.4:c.151C>T MANE Select	NP_001056.1:p.His51Tyr
NM_001346091.2:c.-131-268C>T	NP_001333020.1:n.-131-268C>T
NM_001346092.2:c.-427C>T	NP_001333021.1:n.-427C>T
NR_144351.2:n.413C>T