Canonical Allele Identifier: CA232330862

Gene: TNFRSF1A

Linked Data

• dbSNP Id: rs104895280
• gnomAD v4: 12-6334116-C-A
• MyVariant Identifiers: chr12:g.6443282C>A (hg19) ; chr12:g.6334116C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6334116C>A , CM000674.2:g.6334116C>A	GRCh38
NC_000012.11:g.6443282C>A , CM000674.1:g.6443282C>A	GRCh37
NC_000012.10:g.6313543C>A	NCBI36
NG_007506.1:g.12980G>T , LRG_193:g.12980G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000366159.9:n.202G>T
ENST00000437813.8:c.168G>T	ENSP00000513672.1:p.Ser56=
ENST00000440083.7:c.168G>T	ENSP00000413224.3:p.Ser56=
ENST00000535958.2:c.168G>T	ENSP00000513673.1:p.Ser56=
ENST00000698339.1:c.168G>T	ENSP00000513670.1:p.Ser56=
ENST00000698340.1:c.168G>T	ENSP00000513671.1:p.Ser56=
ENST00000162749.7:c.168G>T MANE Select	ENSP00000162749.2:p.Ser56=
ENST00000162749.6:c.168G>T	ENSP00000162749.2:p.Ser56=
ENST00000366159.8:c.168G>T	ENSP00000380389.3:p.Ser56=
ENST00000437813.7:n.129G>T
ENST00000440083.6:c.168G>T	ENSP00000413224.2:p.Ser56=
ENST00000534885.5:c.40-251G>T	ENSP00000441803.1:n.40-251G>T
ENST00000535958.1:n.389G>T
ENST00000536194.1:c.168G>T	ENSP00000442919.1:p.Ser56=
ENST00000538363.1:n.358G>T
ENST00000539372.5:c.168G>T	ENSP00000442059.1:p.Ser56=
ENST00000540022.5:c.168G>T	ENSP00000438343.1:p.Ser56=
ENST00000543048.5:c.168G>T	ENSP00000439981.1:p.Ser56=
ENST00000543995.5:c.168G>T	ENSP00000442405.1:p.Ser56=
NM_001065.3:c.168G>T , LRG_193t1:c.168G>T	NP_001056.1:p.Ser56=
NM_001346091.1:c.-131-251G>T	NP_001333020.1:n.-131-251G>T
NM_001346092.1:c.-410G>T	NP_001333021.1:n.-410G>T
NR_144351.1:n.471G>T
NM_001065.4:c.168G>T MANE Select	NP_001056.1:p.Ser56=
NM_001346091.2:c.-131-251G>T	NP_001333020.1:n.-131-251G>T
NM_001346092.2:c.-410G>T	NP_001333021.1:n.-410G>T
NR_144351.2:n.430G>T