Canonical Allele Identifier: CA478505026

Gene: TNFRSF1A

Linked Data

• MyVariant Identifiers: chr12:g.6443270G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6334104G>C , CM000674.2:g.6334104G>C	GRCh38
NC_000012.11:g.6443270G>C , CM000674.1:g.6443270G>C	GRCh37
NC_000012.10:g.6313531G>C	NCBI36
NG_007506.1:g.12992C>G , LRG_193:g.12992C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000366159.9:n.214C>G
ENST00000437813.8:c.180C>G	ENSP00000513672.1:p.Thr60=
ENST00000440083.7:c.180C>G	ENSP00000413224.3:p.Thr60=
ENST00000535958.2:c.180C>G	ENSP00000513673.1:p.Thr60=
ENST00000698339.1:c.180C>G	ENSP00000513670.1:p.Thr60=
ENST00000698340.1:c.180C>G	ENSP00000513671.1:p.Thr60=
ENST00000162749.7:c.180C>G MANE Select	ENSP00000162749.2:p.Thr60=
ENST00000162749.6:c.180C>G	ENSP00000162749.2:p.Thr60=
ENST00000366159.8:c.180C>G	ENSP00000380389.3:p.Thr60=
ENST00000437813.7:n.141C>G
ENST00000440083.6:c.180C>G	ENSP00000413224.2:p.Thr60=
ENST00000534885.5:c.40-239C>G	ENSP00000441803.1:n.40-239C>G
ENST00000535958.1:n.401C>G
ENST00000536194.1:c.180C>G	ENSP00000442919.1:p.Thr60=
ENST00000538363.1:n.370C>G
ENST00000539372.5:c.180C>G	ENSP00000442059.1:p.Thr60=
ENST00000540022.5:c.180C>G	ENSP00000438343.1:p.Thr60=
ENST00000543048.5:c.180C>G	ENSP00000439981.1:p.Thr60=
ENST00000543995.5:c.180C>G	ENSP00000442405.1:p.Thr60=
NM_001065.3:c.180C>G , LRG_193t1:c.180C>G	NP_001056.1:p.Thr60=
NM_001346091.1:c.-131-239C>G	NP_001333020.1:n.-131-239C>G
NM_001346092.1:c.-398C>G	NP_001333021.1:n.-398C>G
NR_144351.1:n.483C>G
NM_001065.4:c.180C>G MANE Select	NP_001056.1:p.Thr60=
NM_001346091.2:c.-131-239C>G	NP_001333020.1:n.-131-239C>G
NM_001346092.2:c.-398C>G	NP_001333021.1:n.-398C>G
NR_144351.2:n.442C>G