Canonical Allele Identifier: CA478505068

Gene: TNFRSF1A

Linked Data

• MyVariant Identifiers: chr12:g.6443003G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6333837G>T , CM000674.2:g.6333837G>T	GRCh38
NC_000012.11:g.6443003G>T , CM000674.1:g.6443003G>T	GRCh37
NC_000012.10:g.6313264G>T	NCBI36
NG_007506.1:g.13259C>A , LRG_193:g.13259C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366159.9:n.256C>A
ENST00000437813.8:c.222C>A	ENSP00000513672.1:p.Gly74=
ENST00000440083.7:c.222C>A	ENSP00000413224.3:p.Gly74=
ENST00000535958.2:c.*49C>A	ENSP00000513673.1:n.*49C>A
ENST00000698339.1:c.222C>A	ENSP00000513670.1:p.Gly74=
ENST00000698340.1:c.222C>A	ENSP00000513671.1:p.Gly74=
ENST00000162749.7:c.222C>A MANE Select	ENSP00000162749.2:p.Gly74=
ENST00000162749.6:c.222C>A	ENSP00000162749.2:p.Gly74=
ENST00000366159.8:c.222C>A	ENSP00000380389.3:p.Gly74=
ENST00000437813.7:n.183C>A
ENST00000440083.6:c.222C>A	ENSP00000413224.2:p.Gly74=
ENST00000534885.5:c.68C>A	ENSP00000441803.1:p.Ala23Asp
ENST00000535958.1:n.468C>A
ENST00000536194.1:c.195C>A	ENSP00000442919.1:p.Gly65=
ENST00000539372.5:c.222C>A	ENSP00000442059.1:p.Gly74=
ENST00000540022.5:c.193+254C>A	ENSP00000438343.1:n.193+254C>A
ENST00000543048.5:c.214+8C>A	ENSP00000439981.1:n.214+8C>A
ENST00000543995.5:c.193+254C>A	ENSP00000442405.1:n.193+254C>A
NM_001065.3:c.222C>A , LRG_193t1:c.222C>A	NP_001056.1:p.Gly74=
NM_001346091.1:c.-103C>A	NP_001333020.1:n.-103C>A
NM_001346092.1:c.-356C>A	NP_001333021.1:n.-356C>A
NR_144351.1:n.525C>A
NM_001065.4:c.222C>A MANE Select	NP_001056.1:p.Gly74=
NM_001346091.2:c.-103C>A	NP_001333020.1:n.-103C>A
NM_001346092.2:c.-356C>A	NP_001333021.1:n.-356C>A
NR_144351.2:n.484C>A