Canonical Allele Identifier: CA383548002

Gene: TNFRSF1A

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366159.9:n.1711G>A
ENST00000437813.8:c.*71G>A	ENSP00000513672.1:n.*71G>A
ENST00000440083.7:c.829G>A	ENSP00000413224.3:p.Gly277Ser
ENST00000535038.2:n.792G>A
ENST00000535958.2:c.*437G>A	ENSP00000513673.1:n.*437G>A
ENST00000698337.1:n.459G>A
ENST00000698338.1:n.883G>A
ENST00000698339.1:c.*105G>A	ENSP00000513670.1:n.*105G>A
ENST00000698340.1:c.552-157G>A	ENSP00000513671.1:n.552-157G>A
ENST00000162749.7:c.610G>A MANE Select	ENSP00000162749.2:p.Gly204Ser
ENST00000162749.6:c.610G>A	ENSP00000162749.2:p.Gly204Ser
ENST00000534885.5:c.*87G>A	ENSP00000441803.1:n.*87G>A
ENST00000535038.1:n.280G>A
ENST00000536717.5:n.514G>A
ENST00000537842.5:n.214G>A
ENST00000539372.5:c.610G>A	ENSP00000442059.1:p.Gly204Ser
ENST00000540022.5:c.481G>A	ENSP00000438343.1:p.Gly161Ser
ENST00000543359.5:n.38-157G>A
ENST00000543995.5:c.*197G>A	ENSP00000442405.1:n.*197G>A
NM_001065.3:c.610G>A , LRG_193t1:c.610G>A	NP_001056.1:p.Gly204Ser
NM_001346091.1:c.286G>A	NP_001333020.1:p.Gly96Ser
NM_001346092.1:c.151G>A	NP_001333021.1:p.Gly51Ser
NR_144351.1:n.855-157G>A
NM_001065.4:c.610G>A MANE Select	NP_001056.1:p.Gly204Ser
NM_001346091.2:c.286G>A	NP_001333020.1:p.Gly96Ser
NM_001346092.2:c.151G>A	NP_001333021.1:p.Gly51Ser
NR_144351.2:n.814-157G>A