Canonical Allele Identifier: CA383545619

Gene: TNFRSF1A

Linked Data

• MyVariant Identifiers: chr12:g.6438969G>C (hg19) ; chr12:g.6329803G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6329803G>C , CM000674.2:g.6329803G>C	GRCh38
NC_000012.11:g.6438969G>C , CM000674.1:g.6438969G>C	GRCh37
NC_000012.10:g.6309230G>C	NCBI36
NG_007506.1:g.17293C>G , LRG_193:g.17293C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000366159.9:n.2133C>G
ENST00000437813.8:c.*493C>G	ENSP00000513672.1:n.*493C>G
ENST00000440083.7:c.1251C>G	ENSP00000413224.3:p.Ser417Arg
ENST00000535958.2:c.*859C>G	ENSP00000513673.1:n.*859C>G
ENST00000698337.1:n.993C>G
ENST00000698338.1:n.1646C>G
ENST00000698339.1:c.*527C>G	ENSP00000513670.1:n.*527C>G
ENST00000698340.1:c.*271C>G	ENSP00000513671.1:n.*271C>G
ENST00000162749.7:c.1032C>G MANE Select	ENSP00000162749.2:p.Ser344Arg
ENST00000162749.6:c.1032C>G	ENSP00000162749.2:p.Ser344Arg
ENST00000534885.5:c.*509C>G	ENSP00000441803.1:n.*509C>G
ENST00000536717.5:n.936C>G
ENST00000540022.5:c.903C>G	ENSP00000438343.1:p.Ser301Arg
ENST00000543359.5:n.444C>G
ENST00000543995.5:c.*619C>G	ENSP00000442405.1:n.*619C>G
NM_001065.3:c.1032C>G , LRG_193t1:c.1032C>G	NP_001056.1:p.Ser344Arg
NM_001346091.1:c.708C>G	NP_001333020.1:p.Ser236Arg
NM_001346092.1:c.573C>G	NP_001333021.1:p.Ser191Arg
NR_144351.1:n.1261C>G
NM_001065.4:c.1032C>G MANE Select	NP_001056.1:p.Ser344Arg
NM_001346091.2:c.708C>G	NP_001333020.1:p.Ser236Arg
NM_001346092.2:c.573C>G	NP_001333021.1:p.Ser191Arg
NR_144351.2:n.1220C>G