Canonical Allele Identifier: CA383547687

Gene: TNFRSF1A

Linked Data

• MyVariant Identifiers: chr12:g.6439827A>C (hg19) ; chr12:g.6330661A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6330661A>C , CM000674.2:g.6330661A>C	GRCh38
NC_000012.11:g.6439827A>C , CM000674.1:g.6439827A>C	GRCh37
NC_000012.10:g.6310088A>C	NCBI36
NG_007506.1:g.16435T>G , LRG_193:g.16435T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366159.9:n.1777T>G
ENST00000437813.8:c.*137T>G	ENSP00000513672.1:n.*137T>G
ENST00000440083.7:c.895T>G	ENSP00000413224.3:p.Ser299Ala
ENST00000535038.2:n.858T>G
ENST00000535958.2:c.*503T>G	ENSP00000513673.1:n.*503T>G
ENST00000698337.1:n.666T>G
ENST00000698338.1:n.1090T>G
ENST00000698339.1:c.*171T>G	ENSP00000513670.1:n.*171T>G
ENST00000698340.1:c.602T>G	ENSP00000513671.1:p.Ile201Ser
ENST00000162749.7:c.676T>G MANE Select	ENSP00000162749.2:p.Ser226Ala
ENST00000162749.6:c.676T>G	ENSP00000162749.2:p.Ser226Ala
ENST00000534885.5:c.*153T>G	ENSP00000441803.1:n.*153T>G
ENST00000535038.1:n.487T>G
ENST00000536717.5:n.580T>G
ENST00000537842.5:n.280T>G
ENST00000539372.5:c.676T>G	ENSP00000442059.1:p.Ser226Ala
ENST00000540022.5:c.547T>G	ENSP00000438343.1:p.Ser183Ala
ENST00000543359.5:n.88T>G
ENST00000543995.5:c.*263T>G	ENSP00000442405.1:n.*263T>G
NM_001065.3:c.676T>G , LRG_193t1:c.676T>G	NP_001056.1:p.Ser226Ala
NM_001346091.1:c.352T>G	NP_001333020.1:p.Ser118Ala
NM_001346092.1:c.217T>G	NP_001333021.1:p.Ser73Ala
NR_144351.1:n.905T>G
NM_001065.4:c.676T>G MANE Select	NP_001056.1:p.Ser226Ala
NM_001346091.2:c.352T>G	NP_001333020.1:p.Ser118Ala
NM_001346092.2:c.217T>G	NP_001333021.1:p.Ser73Ala
NR_144351.2:n.864T>G