Canonical Allele Identifier: CA478112727

Gene: TNFRSF1A

Linked Data

• MyVariant Identifiers: chr12:g.6440032G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6330866G>T , CM000674.2:g.6330866G>T	GRCh38
NC_000012.11:g.6440032G>T , CM000674.1:g.6440032G>T	GRCh37
NC_000012.10:g.6310293G>T	NCBI36
NG_007506.1:g.16230C>A , LRG_193:g.16230C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366159.9:n.1713C>A
ENST00000437813.8:c.*73C>A	ENSP00000513672.1:n.*73C>A
ENST00000440083.7:c.831C>A	ENSP00000413224.3:p.Gly277=
ENST00000535038.2:n.794C>A
ENST00000535958.2:c.*439C>A	ENSP00000513673.1:n.*439C>A
ENST00000698337.1:n.461C>A
ENST00000698338.1:n.885C>A
ENST00000698339.1:c.*107C>A	ENSP00000513670.1:n.*107C>A
ENST00000698340.1:c.552-155C>A	ENSP00000513671.1:n.552-155C>A
ENST00000162749.7:c.612C>A MANE Select	ENSP00000162749.2:p.Gly204=
ENST00000162749.6:c.612C>A	ENSP00000162749.2:p.Gly204=
ENST00000534885.5:c.*89C>A	ENSP00000441803.1:n.*89C>A
ENST00000535038.1:n.282C>A
ENST00000536717.5:n.516C>A
ENST00000537842.5:n.216C>A
ENST00000539372.5:c.612C>A	ENSP00000442059.1:p.Gly204=
ENST00000540022.5:c.483C>A	ENSP00000438343.1:p.Gly161=
ENST00000543359.5:n.38-155C>A
ENST00000543995.5:c.*199C>A	ENSP00000442405.1:n.*199C>A
NM_001065.3:c.612C>A , LRG_193t1:c.612C>A	NP_001056.1:p.Gly204=
NM_001346091.1:c.288C>A	NP_001333020.1:p.Gly96=
NM_001346092.1:c.153C>A	NP_001333021.1:p.Gly51=
NR_144351.1:n.855-155C>A
NM_001065.4:c.612C>A MANE Select	NP_001056.1:p.Gly204=
NM_001346091.2:c.288C>A	NP_001333020.1:p.Gly96=
NM_001346092.2:c.153C>A	NP_001333021.1:p.Gly51=
NR_144351.2:n.814-155C>A