Canonical Allele Identifier: CA478505006

Gene: TNFRSF1A

Linked Data

• gnomAD v4: 12-6333783-T-C
• MyVariant Identifiers: chr12:g.6442949T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6333783T>C , CM000674.2:g.6333783T>C	GRCh38
NC_000012.11:g.6442949T>C , CM000674.1:g.6442949T>C	GRCh37
NC_000012.10:g.6313210T>C	NCBI36
NG_007506.1:g.13313A>G , LRG_193:g.13313A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366159.9:n.310A>G
ENST00000437813.8:c.276A>G	ENSP00000513672.1:p.Ser92=
ENST00000440083.7:c.276A>G	ENSP00000413224.3:p.Ser92=
ENST00000535958.2:c.*103A>G	ENSP00000513673.1:n.*103A>G
ENST00000698339.1:c.276A>G	ENSP00000513670.1:p.Ser92=
ENST00000698340.1:c.276A>G	ENSP00000513671.1:p.Ser92=
ENST00000162749.7:c.276A>G MANE Select	ENSP00000162749.2:p.Ser92=
ENST00000162749.6:c.276A>G	ENSP00000162749.2:p.Ser92=
ENST00000366159.8:c.276A>G	ENSP00000380389.3:p.Ser92=
ENST00000437813.7:n.237A>G
ENST00000440083.6:c.276A>G	ENSP00000413224.2:p.Ser92=
ENST00000534885.5:c.122A>G	ENSP00000441803.1:p.Gln41Arg
ENST00000535958.1:n.522A>G
ENST00000536194.1:c.249A>G	ENSP00000442919.1:p.Ser83=
ENST00000539372.5:c.276A>G	ENSP00000442059.1:p.Ser92=
ENST00000540022.5:c.194-267A>G	ENSP00000438343.1:n.194-267A>G
ENST00000543048.5:c.214+62A>G	ENSP00000439981.1:n.214+62A>G
ENST00000543995.5:c.193+308A>G	ENSP00000442405.1:n.193+308A>G
NM_001065.3:c.276A>G , LRG_193t1:c.276A>G	NP_001056.1:p.Ser92=
NM_001346091.1:c.-49A>G	NP_001333020.1:n.-49A>G
NM_001346092.1:c.-302A>G	NP_001333021.1:n.-302A>G
NR_144351.1:n.579A>G
NM_001065.4:c.276A>G MANE Select	NP_001056.1:p.Ser92=
NM_001346091.2:c.-49A>G	NP_001333020.1:n.-49A>G
NM_001346092.2:c.-302A>G	NP_001333021.1:n.-302A>G
NR_144351.2:n.538A>G