Canonical Allele Identifier: CA383548000

Gene: TNFRSF1A

Linked Data

• MyVariant Identifiers: chr12:g.6440034C>A (hg19) ; chr12:g.6330868C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6330868C>A , CM000674.2:g.6330868C>A	GRCh38
NC_000012.11:g.6440034C>A , CM000674.1:g.6440034C>A	GRCh37
NC_000012.10:g.6310295C>A	NCBI36
NG_007506.1:g.16228G>T , LRG_193:g.16228G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366159.9:n.1711G>T
ENST00000437813.8:c.*71G>T	ENSP00000513672.1:n.*71G>T
ENST00000440083.7:c.829G>T	ENSP00000413224.3:p.Gly277Cys
ENST00000535038.2:n.792G>T
ENST00000535958.2:c.*437G>T	ENSP00000513673.1:n.*437G>T
ENST00000698337.1:n.459G>T
ENST00000698338.1:n.883G>T
ENST00000698339.1:c.*105G>T	ENSP00000513670.1:n.*105G>T
ENST00000698340.1:c.552-157G>T	ENSP00000513671.1:n.552-157G>T
ENST00000162749.7:c.610G>T MANE Select	ENSP00000162749.2:p.Gly204Cys
ENST00000162749.6:c.610G>T	ENSP00000162749.2:p.Gly204Cys
ENST00000534885.5:c.*87G>T	ENSP00000441803.1:n.*87G>T
ENST00000535038.1:n.280G>T
ENST00000536717.5:n.514G>T
ENST00000537842.5:n.214G>T
ENST00000539372.5:c.610G>T	ENSP00000442059.1:p.Gly204Cys
ENST00000540022.5:c.481G>T	ENSP00000438343.1:p.Gly161Cys
ENST00000543359.5:n.38-157G>T
ENST00000543995.5:c.*197G>T	ENSP00000442405.1:n.*197G>T
NM_001065.3:c.610G>T , LRG_193t1:c.610G>T	NP_001056.1:p.Gly204Cys
NM_001346091.1:c.286G>T	NP_001333020.1:p.Gly96Cys
NM_001346092.1:c.151G>T	NP_001333021.1:p.Gly51Cys
NR_144351.1:n.855-157G>T
NM_001065.4:c.610G>T MANE Select	NP_001056.1:p.Gly204Cys
NM_001346091.2:c.286G>T	NP_001333020.1:p.Gly96Cys
NM_001346092.2:c.151G>T	NP_001333021.1:p.Gly51Cys
NR_144351.2:n.814-157G>T