Canonical Allele Identifier: CA383548196

Gene: TNFRSF1A

Linked Data

• MyVariant Identifiers: chr12:g.6440091A>C (hg19) ; chr12:g.6330925A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6330925A>C , CM000674.2:g.6330925A>C	GRCh38
NC_000012.11:g.6440091A>C , CM000674.1:g.6440091A>C	GRCh37
NC_000012.10:g.6310352A>C	NCBI36
NG_007506.1:g.16171T>G , LRG_193:g.16171T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366159.9:n.1654T>G
ENST00000437813.8:c.*14T>G	ENSP00000513672.1:n.*14T>G
ENST00000440083.7:c.772T>G	ENSP00000413224.3:p.Cys258Gly
ENST00000535038.2:n.735T>G
ENST00000535958.2:c.*380T>G	ENSP00000513673.1:n.*380T>G
ENST00000698337.1:n.402T>G
ENST00000698338.1:n.826T>G
ENST00000698339.1:c.*48T>G	ENSP00000513670.1:n.*48T>G
ENST00000698340.1:c.552-214T>G	ENSP00000513671.1:n.552-214T>G
ENST00000162749.7:c.553T>G MANE Select	ENSP00000162749.2:p.Cys185Gly
ENST00000162749.6:c.553T>G	ENSP00000162749.2:p.Cys185Gly
ENST00000534885.5:c.*30T>G	ENSP00000441803.1:n.*30T>G
ENST00000535038.1:n.223T>G
ENST00000536717.5:n.457T>G
ENST00000537842.5:n.157T>G
ENST00000539372.5:c.553T>G	ENSP00000442059.1:p.Cys185Gly
ENST00000540022.5:c.424T>G	ENSP00000438343.1:p.Cys142Gly
ENST00000543359.5:n.38-214T>G
ENST00000543995.5:c.*140T>G	ENSP00000442405.1:n.*140T>G
NM_001065.3:c.553T>G , LRG_193t1:c.553T>G	NP_001056.1:p.Cys185Gly
NM_001346091.1:c.229T>G	NP_001333020.1:p.Cys77Gly
NM_001346092.1:c.94T>G	NP_001333021.1:p.Cys32Gly
NR_144351.1:n.855-214T>G
NM_001065.4:c.553T>G MANE Select	NP_001056.1:p.Cys185Gly
NM_001346091.2:c.229T>G	NP_001333020.1:p.Cys77Gly
NM_001346092.2:c.94T>G	NP_001333021.1:p.Cys32Gly
NR_144351.2:n.814-214T>G