Canonical Allele Identifier: CA478112857

Gene: TNFRSF1A

Linked Data

• MyVariant Identifiers: chr12:g.6440068C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6330902C>A , CM000674.2:g.6330902C>A	GRCh38
NC_000012.11:g.6440068C>A , CM000674.1:g.6440068C>A	GRCh37
NC_000012.10:g.6310329C>A	NCBI36
NG_007506.1:g.16194G>T , LRG_193:g.16194G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366159.9:n.1677G>T
ENST00000437813.8:c.*37G>T	ENSP00000513672.1:n.*37G>T
ENST00000440083.7:c.795G>T	ENSP00000413224.3:p.Thr265=
ENST00000535038.2:n.758G>T
ENST00000535958.2:c.*403G>T	ENSP00000513673.1:n.*403G>T
ENST00000698337.1:n.425G>T
ENST00000698338.1:n.849G>T
ENST00000698339.1:c.*71G>T	ENSP00000513670.1:n.*71G>T
ENST00000698340.1:c.552-191G>T	ENSP00000513671.1:n.552-191G>T
ENST00000162749.7:c.576G>T MANE Select	ENSP00000162749.2:p.Thr192=
ENST00000162749.6:c.576G>T	ENSP00000162749.2:p.Thr192=
ENST00000534885.5:c.*53G>T	ENSP00000441803.1:n.*53G>T
ENST00000535038.1:n.246G>T
ENST00000536717.5:n.480G>T
ENST00000537842.5:n.180G>T
ENST00000539372.5:c.576G>T	ENSP00000442059.1:p.Thr192=
ENST00000540022.5:c.447G>T	ENSP00000438343.1:p.Thr149=
ENST00000543359.5:n.38-191G>T
ENST00000543995.5:c.*163G>T	ENSP00000442405.1:n.*163G>T
NM_001065.3:c.576G>T , LRG_193t1:c.576G>T	NP_001056.1:p.Thr192=
NM_001346091.1:c.252G>T	NP_001333020.1:p.Thr84=
NM_001346092.1:c.117G>T	NP_001333021.1:p.Thr39=
NR_144351.1:n.855-191G>T
NM_001065.4:c.576G>T MANE Select	NP_001056.1:p.Thr192=
NM_001346091.2:c.252G>T	NP_001333020.1:p.Thr84=
NM_001346092.2:c.117G>T	NP_001333021.1:p.Thr39=
NR_144351.2:n.814-191G>T