Canonical Allele Identifier: CA6405457

Gene: TNFRSF1A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6330875A>G , CM000674.2:g.6330875A>G	GRCh38
NC_000012.11:g.6440041A>G , CM000674.1:g.6440041A>G	GRCh37
NC_000012.10:g.6310302A>G	NCBI36
NG_007506.1:g.16221T>C , LRG_193:g.16221T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_001065.4:c.603T>C MANE Select	NP_001056.1:p.Asn201=
ENST00000162749.7:c.603T>C MANE Select	ENSP00000162749.2:p.Asn201=
NM_001065.3:c.603T>C , LRG_193t1:c.603T>C	NP_001056.1:p.Asn201=
NM_001346091.1:c.279T>C	NP_001333020.1:p.Asn93=
NM_001346091.2:c.279T>C	NP_001333020.1:p.Asn93=
NM_001346092.1:c.144T>C	NP_001333021.1:p.Asn48=
NM_001346092.2:c.144T>C	NP_001333021.1:p.Asn48=
NR_144351.1:n.855-164T>C
NR_144351.2:n.814-164T>C
ENST00000162749.6:c.603T>C	ENSP00000162749.2:p.Asn201=
ENST00000366159.9:n.1704T>C
ENST00000437813.8:c.*64T>C	ENSP00000513672.1:n.*64T>C
ENST00000440083.7:c.822T>C	ENSP00000413224.3:p.Asn274=
ENST00000534885.5:c.*80T>C	ENSP00000441803.1:n.*80T>C
ENST00000535038.1:n.273T>C
ENST00000535038.2:n.785T>C
ENST00000535958.2:c.*430T>C	ENSP00000513673.1:n.*430T>C
ENST00000536717.5:n.507T>C
ENST00000537842.5:n.207T>C
ENST00000539372.5:c.603T>C	ENSP00000442059.1:p.Asn201=
ENST00000540022.5:c.474T>C	ENSP00000438343.1:p.Asn158=
ENST00000543359.5:n.38-164T>C
ENST00000543995.5:c.*190T>C	ENSP00000442405.1:n.*190T>C
ENST00000698337.1:n.452T>C
ENST00000698338.1:n.876T>C
ENST00000698339.1:c.*98T>C	ENSP00000513670.1:n.*98T>C
ENST00000698340.1:c.552-164T>C	ENSP00000513671.1:n.552-164T>C