Canonical Allele Identifier: CA383548029

Gene: TNFRSF1A

Linked Data

• MyVariant Identifiers: chr12:g.6440046C>A (hg19) ; chr12:g.6330880C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6330880C>A , CM000674.2:g.6330880C>A	GRCh38
NC_000012.11:g.6440046C>A , CM000674.1:g.6440046C>A	GRCh37
NC_000012.10:g.6310307C>A	NCBI36
NG_007506.1:g.16216G>T , LRG_193:g.16216G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366159.9:n.1699G>T
ENST00000437813.8:c.*59G>T	ENSP00000513672.1:n.*59G>T
ENST00000440083.7:c.817G>T	ENSP00000413224.3:p.Glu273Ter
ENST00000535038.2:n.780G>T
ENST00000535958.2:c.*425G>T	ENSP00000513673.1:n.*425G>T
ENST00000698337.1:n.447G>T
ENST00000698338.1:n.871G>T
ENST00000698339.1:c.*93G>T	ENSP00000513670.1:n.*93G>T
ENST00000698340.1:c.552-169G>T	ENSP00000513671.1:n.552-169G>T
ENST00000162749.7:c.598G>T MANE Select	ENSP00000162749.2:p.Glu200Ter
ENST00000162749.6:c.598G>T	ENSP00000162749.2:p.Glu200Ter
ENST00000534885.5:c.*75G>T	ENSP00000441803.1:n.*75G>T
ENST00000535038.1:n.268G>T
ENST00000536717.5:n.502G>T
ENST00000537842.5:n.202G>T
ENST00000539372.5:c.598G>T	ENSP00000442059.1:p.Glu200Ter
ENST00000540022.5:c.469G>T	ENSP00000438343.1:p.Glu157Ter
ENST00000543359.5:n.38-169G>T
ENST00000543995.5:c.*185G>T	ENSP00000442405.1:n.*185G>T
NM_001065.3:c.598G>T , LRG_193t1:c.598G>T	NP_001056.1:p.Glu200Ter
NM_001346091.1:c.274G>T	NP_001333020.1:p.Glu92Ter
NM_001346092.1:c.139G>T	NP_001333021.1:p.Glu47Ter
NR_144351.1:n.855-169G>T
NM_001065.4:c.598G>T MANE Select	NP_001056.1:p.Glu200Ter
NM_001346091.2:c.274G>T	NP_001333020.1:p.Glu92Ter
NM_001346092.2:c.139G>T	NP_001333021.1:p.Glu47Ter
NR_144351.2:n.814-169G>T