Canonical Allele Identifier: CA383545908

Gene: TNFRSF1A

Linked Data

• MyVariant Identifiers: chr12:g.6439089A>C (hg19) ; chr12:g.6329923A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6329923A>C , CM000674.2:g.6329923A>C	GRCh38
NC_000012.11:g.6439089A>C , CM000674.1:g.6439089A>C	GRCh37
NC_000012.10:g.6309350A>C	NCBI36
NG_007506.1:g.17173T>G , LRG_193:g.17173T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000366159.9:n.2013T>G
ENST00000437813.8:c.*373T>G	ENSP00000513672.1:n.*373T>G
ENST00000440083.7:c.1131T>G	ENSP00000413224.3:p.Cys377Trp
ENST00000535958.2:c.*739T>G	ENSP00000513673.1:n.*739T>G
ENST00000698337.1:n.873T>G
ENST00000698338.1:n.1526T>G
ENST00000698339.1:c.*407T>G	ENSP00000513670.1:n.*407T>G
ENST00000698340.1:c.*151T>G	ENSP00000513671.1:n.*151T>G
ENST00000162749.7:c.912T>G MANE Select	ENSP00000162749.2:p.Cys304Trp
ENST00000162749.6:c.912T>G	ENSP00000162749.2:p.Cys304Trp
ENST00000534885.5:c.*389T>G	ENSP00000441803.1:n.*389T>G
ENST00000536717.5:n.816T>G
ENST00000537842.5:n.373-24T>G
ENST00000540022.5:c.783T>G	ENSP00000438343.1:p.Cys261Trp
ENST00000543359.5:n.324T>G
ENST00000543995.5:c.*499T>G	ENSP00000442405.1:n.*499T>G
NM_001065.3:c.912T>G , LRG_193t1:c.912T>G	NP_001056.1:p.Cys304Trp
NM_001346091.1:c.588T>G	NP_001333020.1:p.Cys196Trp
NM_001346092.1:c.453T>G	NP_001333021.1:p.Cys151Trp
NR_144351.1:n.1141T>G
NM_001065.4:c.912T>G MANE Select	NP_001056.1:p.Cys304Trp
NM_001346091.2:c.588T>G	NP_001333020.1:p.Cys196Trp
NM_001346092.2:c.453T>G	NP_001333021.1:p.Cys151Trp
NR_144351.2:n.1100T>G