Canonical Allele Identifier: CA383547998

Gene: TNFRSF1A

Linked Data

• MyVariant Identifiers: chr12:g.6440033C>G (hg19) ; chr12:g.6330867C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6330867C>G , CM000674.2:g.6330867C>G	GRCh38
NC_000012.11:g.6440033C>G , CM000674.1:g.6440033C>G	GRCh37
NC_000012.10:g.6310294C>G	NCBI36
NG_007506.1:g.16229G>C , LRG_193:g.16229G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366159.9:n.1712G>C
ENST00000437813.8:c.*72G>C	ENSP00000513672.1:n.*72G>C
ENST00000440083.7:c.830G>C	ENSP00000413224.3:p.Gly277Ala
ENST00000535038.2:n.793G>C
ENST00000535958.2:c.*438G>C	ENSP00000513673.1:n.*438G>C
ENST00000698337.1:n.460G>C
ENST00000698338.1:n.884G>C
ENST00000698339.1:c.*106G>C	ENSP00000513670.1:n.*106G>C
ENST00000698340.1:c.552-156G>C	ENSP00000513671.1:n.552-156G>C
ENST00000162749.7:c.611G>C MANE Select	ENSP00000162749.2:p.Gly204Ala
ENST00000162749.6:c.611G>C	ENSP00000162749.2:p.Gly204Ala
ENST00000534885.5:c.*88G>C	ENSP00000441803.1:n.*88G>C
ENST00000535038.1:n.281G>C
ENST00000536717.5:n.515G>C
ENST00000537842.5:n.215G>C
ENST00000539372.5:c.611G>C	ENSP00000442059.1:p.Gly204Ala
ENST00000540022.5:c.482G>C	ENSP00000438343.1:p.Gly161Ala
ENST00000543359.5:n.38-156G>C
ENST00000543995.5:c.*198G>C	ENSP00000442405.1:n.*198G>C
NM_001065.3:c.611G>C , LRG_193t1:c.611G>C	NP_001056.1:p.Gly204Ala
NM_001346091.1:c.287G>C	NP_001333020.1:p.Gly96Ala
NM_001346092.1:c.152G>C	NP_001333021.1:p.Gly51Ala
NR_144351.1:n.855-156G>C
NM_001065.4:c.611G>C MANE Select	NP_001056.1:p.Gly204Ala
NM_001346091.2:c.287G>C	NP_001333020.1:p.Gly96Ala
NM_001346092.2:c.152G>C	NP_001333021.1:p.Gly51Ala
NR_144351.2:n.814-156G>C