Canonical Allele Identifier: CA383550056

Gene: TNFRSF1A

Linked Data

• MyVariant Identifiers: chr12:g.6442597C>A (hg19) ; chr12:g.6333431C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6333431C>A , CM000674.2:g.6333431C>A	GRCh38
NC_000012.11:g.6442597C>A , CM000674.1:g.6442597C>A	GRCh37
NC_000012.10:g.6312858C>A	NCBI36
NG_007506.1:g.13665G>T , LRG_193:g.13665G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366159.9:n.442G>T
ENST00000437813.8:c.408G>T	ENSP00000513672.1:p.Trp136Cys
ENST00000440083.7:c.408G>T	ENSP00000413224.3:p.Trp136Cys
ENST00000535958.2:c.*235G>T	ENSP00000513673.1:n.*235G>T
ENST00000698339.1:c.408G>T	ENSP00000513670.1:p.Trp136Cys
ENST00000698340.1:c.408G>T	ENSP00000513671.1:p.Trp136Cys
ENST00000162749.7:c.408G>T MANE Select	ENSP00000162749.2:p.Trp136Cys
ENST00000162749.6:c.408G>T	ENSP00000162749.2:p.Trp136Cys
ENST00000366159.8:c.408G>T	ENSP00000380389.3:p.Trp136Cys
ENST00000437813.7:n.369G>T
ENST00000440083.6:c.408G>T	ENSP00000413224.2:p.Trp136Cys
ENST00000534885.5:c.254G>T	ENSP00000441803.1:p.Gly85Val
ENST00000537842.5:n.12G>T
ENST00000539372.5:c.408G>T	ENSP00000442059.1:p.Trp136Cys
ENST00000540022.5:c.279G>T	ENSP00000438343.1:p.Trp93Cys
ENST00000543048.5:c.*19G>T	ENSP00000439981.1:n.*19G>T
ENST00000543995.5:c.214G>T	ENSP00000442405.1:p.Glu72Ter
NM_001065.3:c.408G>T , LRG_193t1:c.408G>T	NP_001056.1:p.Trp136Cys
NM_001346091.1:c.84G>T	NP_001333020.1:p.Trp28Cys
NM_001346092.1:c.-170G>T	NP_001333021.1:n.-170G>T
NR_144351.1:n.711G>T
NM_001065.4:c.408G>T MANE Select	NP_001056.1:p.Trp136Cys
NM_001346091.2:c.84G>T	NP_001333020.1:p.Trp28Cys
NM_001346092.2:c.-170G>T	NP_001333021.1:n.-170G>T
NR_144351.2:n.670G>T