Canonical Allele Identifier: CA478504903

Gene: TNFRSF1A

Linked Data

• MyVariant Identifiers: chr12:g.6442603A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6333437A>G , CM000674.2:g.6333437A>G	GRCh38
NC_000012.11:g.6442603A>G , CM000674.1:g.6442603A>G	GRCh37
NC_000012.10:g.6312864A>G	NCBI36
NG_007506.1:g.13659T>C , LRG_193:g.13659T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366159.9:n.436T>C
ENST00000437813.8:c.402T>C	ENSP00000513672.1:p.His134=
ENST00000440083.7:c.402T>C	ENSP00000413224.3:p.His134=
ENST00000535958.2:c.*229T>C	ENSP00000513673.1:n.*229T>C
ENST00000698339.1:c.402T>C	ENSP00000513670.1:p.His134=
ENST00000698340.1:c.402T>C	ENSP00000513671.1:p.His134=
ENST00000162749.7:c.402T>C MANE Select	ENSP00000162749.2:p.His134=
ENST00000162749.6:c.402T>C	ENSP00000162749.2:p.His134=
ENST00000366159.8:c.402T>C	ENSP00000380389.3:p.His134=
ENST00000437813.7:n.363T>C
ENST00000440083.6:c.402T>C	ENSP00000413224.2:p.His134=
ENST00000534885.5:c.248T>C	ENSP00000441803.1:p.Ile83Thr
ENST00000537842.5:n.6T>C
ENST00000539372.5:c.402T>C	ENSP00000442059.1:p.His134=
ENST00000540022.5:c.273T>C	ENSP00000438343.1:p.His91=
ENST00000543048.5:c.*13T>C	ENSP00000439981.1:n.*13T>C
ENST00000543995.5:c.208T>C	ENSP00000442405.1:p.Leu70=
NM_001065.3:c.402T>C , LRG_193t1:c.402T>C	NP_001056.1:p.His134=
NM_001346091.1:c.78T>C	NP_001333020.1:p.His26=
NM_001346092.1:c.-176T>C	NP_001333021.1:n.-176T>C
NR_144351.1:n.705T>C
NM_001065.4:c.402T>C MANE Select	NP_001056.1:p.His134=
NM_001346091.2:c.78T>C	NP_001333020.1:p.His26=
NM_001346092.2:c.-176T>C	NP_001333021.1:n.-176T>C
NR_144351.2:n.664T>C