Canonical Allele Identifier: CA478504760

Gene: TNFRSF1A

Linked Data

• MyVariant Identifiers: chr12:g.6438981C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6329815C>T , CM000674.2:g.6329815C>T	GRCh38
NC_000012.11:g.6438981C>T , CM000674.1:g.6438981C>T	GRCh37
NC_000012.10:g.6309242C>T	NCBI36
NG_007506.1:g.17281G>A , LRG_193:g.17281G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000366159.9:n.2121G>A
ENST00000437813.8:c.*481G>A	ENSP00000513672.1:n.*481G>A
ENST00000440083.7:c.1239G>A	ENSP00000413224.3:p.Lys413=
ENST00000535958.2:c.*847G>A	ENSP00000513673.1:n.*847G>A
ENST00000698337.1:n.981G>A
ENST00000698338.1:n.1634G>A
ENST00000698339.1:c.*515G>A	ENSP00000513670.1:n.*515G>A
ENST00000698340.1:c.*259G>A	ENSP00000513671.1:n.*259G>A
ENST00000162749.7:c.1020G>A MANE Select	ENSP00000162749.2:p.Lys340=
ENST00000162749.6:c.1020G>A	ENSP00000162749.2:p.Lys340=
ENST00000534885.5:c.*497G>A	ENSP00000441803.1:n.*497G>A
ENST00000536717.5:n.924G>A
ENST00000540022.5:c.891G>A	ENSP00000438343.1:p.Lys297=
ENST00000543359.5:n.432G>A
ENST00000543995.5:c.*607G>A	ENSP00000442405.1:n.*607G>A
NM_001065.3:c.1020G>A , LRG_193t1:c.1020G>A	NP_001056.1:p.Lys340=
NM_001346091.1:c.696G>A	NP_001333020.1:p.Lys232=
NM_001346092.1:c.561G>A	NP_001333021.1:p.Lys187=
NR_144351.1:n.1249G>A
NM_001065.4:c.1020G>A MANE Select	NP_001056.1:p.Lys340=
NM_001346091.2:c.696G>A	NP_001333020.1:p.Lys232=
NM_001346092.2:c.561G>A	NP_001333021.1:p.Lys187=
NR_144351.2:n.1208G>A