Canonical Allele Identifier: CA383548025

Gene: TNFRSF1A

Linked Data

• MyVariant Identifiers: chr12:g.6440044C>G (hg19) ; chr12:g.6330878C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6330878C>G , CM000674.2:g.6330878C>G	GRCh38
NC_000012.11:g.6440044C>G , CM000674.1:g.6440044C>G	GRCh37
NC_000012.10:g.6310305C>G	NCBI36
NG_007506.1:g.16218G>C , LRG_193:g.16218G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366159.9:n.1701G>C
ENST00000437813.8:c.*61G>C	ENSP00000513672.1:n.*61G>C
ENST00000440083.7:c.819G>C	ENSP00000413224.3:p.Glu273Asp
ENST00000535038.2:n.782G>C
ENST00000535958.2:c.*427G>C	ENSP00000513673.1:n.*427G>C
ENST00000698337.1:n.449G>C
ENST00000698338.1:n.873G>C
ENST00000698339.1:c.*95G>C	ENSP00000513670.1:n.*95G>C
ENST00000698340.1:c.552-167G>C	ENSP00000513671.1:n.552-167G>C
ENST00000162749.7:c.600G>C MANE Select	ENSP00000162749.2:p.Glu200Asp
ENST00000162749.6:c.600G>C	ENSP00000162749.2:p.Glu200Asp
ENST00000534885.5:c.*77G>C	ENSP00000441803.1:n.*77G>C
ENST00000535038.1:n.270G>C
ENST00000536717.5:n.504G>C
ENST00000537842.5:n.204G>C
ENST00000539372.5:c.600G>C	ENSP00000442059.1:p.Glu200Asp
ENST00000540022.5:c.471G>C	ENSP00000438343.1:p.Glu157Asp
ENST00000543359.5:n.38-167G>C
ENST00000543995.5:c.*187G>C	ENSP00000442405.1:n.*187G>C
NM_001065.3:c.600G>C , LRG_193t1:c.600G>C	NP_001056.1:p.Glu200Asp
NM_001346091.1:c.276G>C	NP_001333020.1:p.Glu92Asp
NM_001346092.1:c.141G>C	NP_001333021.1:p.Glu47Asp
NR_144351.1:n.855-167G>C
NM_001065.4:c.600G>C MANE Select	NP_001056.1:p.Glu200Asp
NM_001346091.2:c.276G>C	NP_001333020.1:p.Glu92Asp
NM_001346092.2:c.141G>C	NP_001333021.1:p.Glu47Asp
NR_144351.2:n.814-167G>C