Canonical Allele Identifier: CA478112713

Gene: TNFRSF1A

Linked Data

• MyVariant Identifiers: chr12:g.6440029A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6330863A>T , CM000674.2:g.6330863A>T	GRCh38
NC_000012.11:g.6440029A>T , CM000674.1:g.6440029A>T	GRCh37
NC_000012.10:g.6310290A>T	NCBI36
NG_007506.1:g.16233T>A , LRG_193:g.16233T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366159.9:n.1716T>A
ENST00000437813.8:c.*76T>A	ENSP00000513672.1:n.*76T>A
ENST00000440083.7:c.834T>A	ENSP00000413224.3:p.Thr278=
ENST00000535038.2:n.797T>A
ENST00000535958.2:c.*442T>A	ENSP00000513673.1:n.*442T>A
ENST00000698337.1:n.464T>A
ENST00000698338.1:n.888T>A
ENST00000698339.1:c.*110T>A	ENSP00000513670.1:n.*110T>A
ENST00000698340.1:c.552-152T>A	ENSP00000513671.1:n.552-152T>A
ENST00000162749.7:c.615T>A MANE Select	ENSP00000162749.2:p.Thr205=
ENST00000162749.6:c.615T>A	ENSP00000162749.2:p.Thr205=
ENST00000534885.5:c.*92T>A	ENSP00000441803.1:n.*92T>A
ENST00000535038.1:n.285T>A
ENST00000536717.5:n.519T>A
ENST00000537842.5:n.219T>A
ENST00000539372.5:c.615T>A	ENSP00000442059.1:p.Thr205=
ENST00000540022.5:c.486T>A	ENSP00000438343.1:p.Thr162=
ENST00000543359.5:n.38-152T>A
ENST00000543995.5:c.*202T>A	ENSP00000442405.1:n.*202T>A
NM_001065.3:c.615T>A , LRG_193t1:c.615T>A	NP_001056.1:p.Thr205=
NM_001346091.1:c.291T>A	NP_001333020.1:p.Thr97=
NM_001346092.1:c.156T>A	NP_001333021.1:p.Thr52=
NR_144351.1:n.855-152T>A
NM_001065.4:c.615T>A MANE Select	NP_001056.1:p.Thr205=
NM_001346091.2:c.291T>A	NP_001333020.1:p.Thr97=
NM_001346092.2:c.156T>A	NP_001333021.1:p.Thr52=
NR_144351.2:n.814-152T>A