Canonical Allele Identifier: CA383545914

Gene: TNFRSF1A

Linked Data

• MyVariant Identifiers: chr12:g.6439091A>G (hg19) ; chr12:g.6329925A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6329925A>G , CM000674.2:g.6329925A>G	GRCh38
NC_000012.11:g.6439091A>G , CM000674.1:g.6439091A>G	GRCh37
NC_000012.10:g.6309352A>G	NCBI36
NG_007506.1:g.17171T>C , LRG_193:g.17171T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366159.9:n.2011T>C
ENST00000437813.8:c.*371T>C	ENSP00000513672.1:n.*371T>C
ENST00000440083.7:c.1129T>C	ENSP00000413224.3:p.Cys377Arg
ENST00000535958.2:c.*737T>C	ENSP00000513673.1:n.*737T>C
ENST00000698337.1:n.871T>C
ENST00000698338.1:n.1524T>C
ENST00000698339.1:c.*405T>C	ENSP00000513670.1:n.*405T>C
ENST00000698340.1:c.*149T>C	ENSP00000513671.1:n.*149T>C
ENST00000162749.7:c.910T>C MANE Select	ENSP00000162749.2:p.Cys304Arg
ENST00000162749.6:c.910T>C	ENSP00000162749.2:p.Cys304Arg
ENST00000534885.5:c.*387T>C	ENSP00000441803.1:n.*387T>C
ENST00000536717.5:n.814T>C
ENST00000537842.5:n.373-26T>C
ENST00000540022.5:c.781T>C	ENSP00000438343.1:p.Cys261Arg
ENST00000543359.5:n.322T>C
ENST00000543995.5:c.*497T>C	ENSP00000442405.1:n.*497T>C
NM_001065.3:c.910T>C , LRG_193t1:c.910T>C	NP_001056.1:p.Cys304Arg
NM_001346091.1:c.586T>C	NP_001333020.1:p.Cys196Arg
NM_001346092.1:c.451T>C	NP_001333021.1:p.Cys151Arg
NR_144351.1:n.1139T>C
NM_001065.4:c.910T>C MANE Select	NP_001056.1:p.Cys304Arg
NM_001346091.2:c.586T>C	NP_001333020.1:p.Cys196Arg
NM_001346092.2:c.451T>C	NP_001333021.1:p.Cys151Arg
NR_144351.2:n.1098T>C