Canonical Allele Identifier: CA383550632

Gene: TNFRSF1A

Linked Data

• MyVariant Identifiers: chr12:g.6442985G>C (hg19) ; chr12:g.6333819G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6333819G>C , CM000674.2:g.6333819G>C	GRCh38
NC_000012.11:g.6442985G>C , CM000674.1:g.6442985G>C	GRCh37
NC_000012.10:g.6313246G>C	NCBI36
NG_007506.1:g.13277C>G , LRG_193:g.13277C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366159.9:n.274C>G
ENST00000437813.8:c.240C>G	ENSP00000513672.1:p.Asp80Glu
ENST00000440083.7:c.240C>G	ENSP00000413224.3:p.Asp80Glu
ENST00000535958.2:c.*67C>G	ENSP00000513673.1:n.*67C>G
ENST00000698339.1:c.240C>G	ENSP00000513670.1:p.Asp80Glu
ENST00000698340.1:c.240C>G	ENSP00000513671.1:p.Asp80Glu
ENST00000162749.7:c.240C>G MANE Select	ENSP00000162749.2:p.Asp80Glu
ENST00000162749.6:c.240C>G	ENSP00000162749.2:p.Asp80Glu
ENST00000366159.8:c.240C>G	ENSP00000380389.3:p.Asp80Glu
ENST00000437813.7:n.201C>G
ENST00000440083.6:c.240C>G	ENSP00000413224.2:p.Asp80Glu
ENST00000534885.5:c.86C>G	ENSP00000441803.1:p.Thr29Ser
ENST00000535958.1:n.486C>G
ENST00000536194.1:c.213C>G	ENSP00000442919.1:p.Asp71Glu
ENST00000539372.5:c.240C>G	ENSP00000442059.1:p.Asp80Glu
ENST00000540022.5:c.193+272C>G	ENSP00000438343.1:n.193+272C>G
ENST00000543048.5:c.214+26C>G	ENSP00000439981.1:n.214+26C>G
ENST00000543995.5:c.193+272C>G	ENSP00000442405.1:n.193+272C>G
NM_001065.3:c.240C>G , LRG_193t1:c.240C>G	NP_001056.1:p.Asp80Glu
NM_001346091.1:c.-85C>G	NP_001333020.1:n.-85C>G
NM_001346092.1:c.-338C>G	NP_001333021.1:n.-338C>G
NR_144351.1:n.543C>G
NM_001065.4:c.240C>G MANE Select	NP_001056.1:p.Asp80Glu
NM_001346091.2:c.-85C>G	NP_001333020.1:n.-85C>G
NM_001346092.2:c.-338C>G	NP_001333021.1:n.-338C>G
NR_144351.2:n.502C>G