Canonical Allele Identifier: CA478112823

Gene: TNFRSF1A

Linked Data

• MyVariant Identifiers: chr12:g.6440058G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6330892G>A , CM000674.2:g.6330892G>A	GRCh38
NC_000012.11:g.6440058G>A , CM000674.1:g.6440058G>A	GRCh37
NC_000012.10:g.6310319G>A	NCBI36
NG_007506.1:g.16204C>T , LRG_193:g.16204C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366159.9:n.1687C>T
ENST00000437813.8:c.*47C>T	ENSP00000513672.1:n.*47C>T
ENST00000440083.7:c.805C>T	ENSP00000413224.3:p.Leu269=
ENST00000535038.2:n.768C>T
ENST00000535958.2:c.*413C>T	ENSP00000513673.1:n.*413C>T
ENST00000698337.1:n.435C>T
ENST00000698338.1:n.859C>T
ENST00000698339.1:c.*81C>T	ENSP00000513670.1:n.*81C>T
ENST00000698340.1:c.552-181C>T	ENSP00000513671.1:n.552-181C>T
ENST00000162749.7:c.586C>T MANE Select	ENSP00000162749.2:p.Leu196=
ENST00000162749.6:c.586C>T	ENSP00000162749.2:p.Leu196=
ENST00000534885.5:c.*63C>T	ENSP00000441803.1:n.*63C>T
ENST00000535038.1:n.256C>T
ENST00000536717.5:n.490C>T
ENST00000537842.5:n.190C>T
ENST00000539372.5:c.586C>T	ENSP00000442059.1:p.Leu196=
ENST00000540022.5:c.457C>T	ENSP00000438343.1:p.Leu153=
ENST00000543359.5:n.38-181C>T
ENST00000543995.5:c.*173C>T	ENSP00000442405.1:n.*173C>T
NM_001065.3:c.586C>T , LRG_193t1:c.586C>T	NP_001056.1:p.Leu196=
NM_001346091.1:c.262C>T	NP_001333020.1:p.Leu88=
NM_001346092.1:c.127C>T	NP_001333021.1:p.Leu43=
NR_144351.1:n.855-181C>T
NM_001065.4:c.586C>T MANE Select	NP_001056.1:p.Leu196=
NM_001346091.2:c.262C>T	NP_001333020.1:p.Leu88=
NM_001346092.2:c.127C>T	NP_001333021.1:p.Leu43=
NR_144351.2:n.814-181C>T