Canonical Allele Identifier: CA478113160

Gene: TNFRSF1A

Linked Data

• MyVariant Identifiers: chr12:g.6443363T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6334197T>G , CM000674.2:g.6334197T>G	GRCh38
NC_000012.11:g.6443363T>G , CM000674.1:g.6443363T>G	GRCh37
NC_000012.10:g.6313624T>G	NCBI36
NG_007506.1:g.12899A>C , LRG_193:g.12899A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366159.9:n.121A>C
ENST00000437813.8:c.87A>C	ENSP00000513672.1:p.Gly29=
ENST00000440083.7:c.87A>C	ENSP00000413224.3:p.Gly29=
ENST00000535958.2:c.87A>C	ENSP00000513673.1:p.Gly29=
ENST00000698339.1:c.87A>C	ENSP00000513670.1:p.Gly29=
ENST00000698340.1:c.87A>C	ENSP00000513671.1:p.Gly29=
ENST00000162749.7:c.87A>C MANE Select	ENSP00000162749.2:p.Gly29=
ENST00000162749.6:c.87A>C	ENSP00000162749.2:p.Gly29=
ENST00000366159.8:c.87A>C	ENSP00000380389.3:p.Gly29=
ENST00000437813.7:n.48A>C
ENST00000440083.6:c.87A>C	ENSP00000413224.2:p.Gly29=
ENST00000534885.5:c.40-332A>C	ENSP00000441803.1:n.40-332A>C
ENST00000535958.1:n.308A>C
ENST00000536194.1:c.87A>C	ENSP00000442919.1:p.Gly29=
ENST00000538363.1:n.277A>C
ENST00000539372.5:c.87A>C	ENSP00000442059.1:p.Gly29=
ENST00000540022.5:c.87A>C	ENSP00000438343.1:p.Gly29=
ENST00000543048.5:c.87A>C	ENSP00000439981.1:p.Gly29=
ENST00000543995.5:c.87A>C	ENSP00000442405.1:p.Gly29=
NM_001065.3:c.87A>C , LRG_193t1:c.87A>C	NP_001056.1:p.Gly29=
NM_001346091.1:c.-131-332A>C	NP_001333020.1:n.-131-332A>C
NM_001346092.1:c.-491A>C	NP_001333021.1:n.-491A>C
NR_144351.1:n.390A>C
NM_001065.4:c.87A>C MANE Select	NP_001056.1:p.Gly29=
NM_001346091.2:c.-131-332A>C	NP_001333020.1:n.-131-332A>C
NM_001346092.2:c.-491A>C	NP_001333021.1:n.-491A>C
NR_144351.2:n.349A>C