Canonical Allele Identifier: CA383548022

Gene: TNFRSF1A

Linked Data

• MyVariant Identifiers: chr12:g.6440043T>C (hg19) ; chr12:g.6330877T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6330877T>C , CM000674.2:g.6330877T>C	GRCh38
NC_000012.11:g.6440043T>C , CM000674.1:g.6440043T>C	GRCh37
NC_000012.10:g.6310304T>C	NCBI36
NG_007506.1:g.16219A>G , LRG_193:g.16219A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366159.9:n.1702A>G
ENST00000437813.8:c.*62A>G	ENSP00000513672.1:n.*62A>G
ENST00000440083.7:c.820A>G	ENSP00000413224.3:p.Asn274Asp
ENST00000535038.2:n.783A>G
ENST00000535958.2:c.*428A>G	ENSP00000513673.1:n.*428A>G
ENST00000698337.1:n.450A>G
ENST00000698338.1:n.874A>G
ENST00000698339.1:c.*96A>G	ENSP00000513670.1:n.*96A>G
ENST00000698340.1:c.552-166A>G	ENSP00000513671.1:n.552-166A>G
ENST00000162749.7:c.601A>G MANE Select	ENSP00000162749.2:p.Asn201Asp
ENST00000162749.6:c.601A>G	ENSP00000162749.2:p.Asn201Asp
ENST00000534885.5:c.*78A>G	ENSP00000441803.1:n.*78A>G
ENST00000535038.1:n.271A>G
ENST00000536717.5:n.505A>G
ENST00000537842.5:n.205A>G
ENST00000539372.5:c.601A>G	ENSP00000442059.1:p.Asn201Asp
ENST00000540022.5:c.472A>G	ENSP00000438343.1:p.Asn158Asp
ENST00000543359.5:n.38-166A>G
ENST00000543995.5:c.*188A>G	ENSP00000442405.1:n.*188A>G
NM_001065.3:c.601A>G , LRG_193t1:c.601A>G	NP_001056.1:p.Asn201Asp
NM_001346091.1:c.277A>G	NP_001333020.1:p.Asn93Asp
NM_001346092.1:c.142A>G	NP_001333021.1:p.Asn48Asp
NR_144351.1:n.855-166A>G
NM_001065.4:c.601A>G MANE Select	NP_001056.1:p.Asn201Asp
NM_001346091.2:c.277A>G	NP_001333020.1:p.Asn93Asp
NM_001346092.2:c.142A>G	NP_001333021.1:p.Asn48Asp
NR_144351.2:n.814-166A>G