Canonical Allele Identifier: CA383549121

Gene: TNFRSF1A

Linked Data

• MyVariant Identifiers: chr12:g.6442295G>C (hg19) ; chr12:g.6333129G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6333129G>C , CM000674.2:g.6333129G>C	GRCh38
NC_000012.11:g.6442295G>C , CM000674.1:g.6442295G>C	GRCh37
NC_000012.10:g.6312556G>C	NCBI36
NG_007506.1:g.13967C>G , LRG_193:g.13967C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366159.9:n.525C>G
ENST00000437813.8:c.491C>G	ENSP00000513672.1:p.Thr164Ser
ENST00000440083.7:c.710C>G	ENSP00000413224.3:p.Thr237Ser
ENST00000535958.2:c.*318C>G	ENSP00000513673.1:n.*318C>G
ENST00000698339.1:c.491C>G	ENSP00000513670.1:p.Thr164Ser
ENST00000698340.1:c.491C>G	ENSP00000513671.1:p.Thr164Ser
ENST00000162749.7:c.491C>G MANE Select	ENSP00000162749.2:p.Thr164Ser
ENST00000162749.6:c.491C>G	ENSP00000162749.2:p.Thr164Ser
ENST00000366159.8:c.491C>G	ENSP00000380389.3:p.Thr164Ser
ENST00000437813.7:n.452C>G
ENST00000440083.6:c.710C>G	ENSP00000413224.2:p.Thr237Ser
ENST00000534885.5:c.337C>G	ENSP00000441803.1:p.Pro113Ala
ENST00000537842.5:n.95C>G
ENST00000539372.5:c.491C>G	ENSP00000442059.1:p.Thr164Ser
ENST00000540022.5:c.362C>G	ENSP00000438343.1:p.Thr121Ser
ENST00000543048.5:c.*102C>G	ENSP00000439981.1:n.*102C>G
ENST00000543995.5:c.*78C>G	ENSP00000442405.1:n.*78C>G
NM_001065.3:c.491C>G , LRG_193t1:c.491C>G	NP_001056.1:p.Thr164Ser
NM_001346091.1:c.167C>G	NP_001333020.1:p.Thr56Ser
NM_001346092.1:c.-87C>G	NP_001333021.1:n.-87C>G
NR_144351.1:n.794C>G
NM_001065.4:c.491C>G MANE Select	NP_001056.1:p.Thr164Ser
NM_001346091.2:c.167C>G	NP_001333020.1:p.Thr56Ser
NM_001346092.2:c.-87C>G	NP_001333021.1:n.-87C>G
NR_144351.2:n.753C>G