Canonical Allele Identifier: CA478112363

Gene: TNFRSF1A

Linked Data

• MyVariant Identifiers: chr12:g.6439810A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6330644A>T , CM000674.2:g.6330644A>T	GRCh38
NC_000012.11:g.6439810A>T , CM000674.1:g.6439810A>T	GRCh37
NC_000012.10:g.6310071A>T	NCBI36
NG_007506.1:g.16452T>A , LRG_193:g.16452T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366159.9:n.1794T>A
ENST00000437813.8:c.*154T>A	ENSP00000513672.1:n.*154T>A
ENST00000440083.7:c.912T>A	ENSP00000413224.3:p.Gly304=
ENST00000535038.2:n.875T>A
ENST00000535958.2:c.*520T>A	ENSP00000513673.1:n.*520T>A
ENST00000698337.1:n.683T>A
ENST00000698338.1:n.1107T>A
ENST00000698339.1:c.*188T>A	ENSP00000513670.1:n.*188T>A
ENST00000698340.1:c.619T>A	ENSP00000513671.1:p.Phe207Ile
ENST00000162749.7:c.693T>A MANE Select	ENSP00000162749.2:p.Gly231=
ENST00000162749.6:c.693T>A	ENSP00000162749.2:p.Gly231=
ENST00000534885.5:c.*170T>A	ENSP00000441803.1:n.*170T>A
ENST00000535038.1:n.504T>A
ENST00000536717.5:n.597T>A
ENST00000537842.5:n.297T>A
ENST00000539372.5:c.693T>A	ENSP00000442059.1:p.Gly231=
ENST00000540022.5:c.564T>A	ENSP00000438343.1:p.Gly188=
ENST00000543359.5:n.105T>A
ENST00000543995.5:c.*280T>A	ENSP00000442405.1:n.*280T>A
NM_001065.3:c.693T>A , LRG_193t1:c.693T>A	NP_001056.1:p.Gly231=
NM_001346091.1:c.369T>A	NP_001333020.1:p.Gly123=
NM_001346092.1:c.234T>A	NP_001333021.1:p.Gly78=
NR_144351.1:n.922T>A
NM_001065.4:c.693T>A MANE Select	NP_001056.1:p.Gly231=
NM_001346091.2:c.369T>A	NP_001333020.1:p.Gly123=
NM_001346092.2:c.234T>A	NP_001333021.1:p.Gly78=
NR_144351.2:n.881T>A