Canonical Allele Identifier: CA2014024025

Gene: TNFRSF1A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6330680G= , CM000674.2:g.6330680G=	GRCh38
NC_000012.11:g.6439846G= , CM000674.1:g.6439846G=	GRCh37
NC_000012.10:g.6310107G=	NCBI36
NG_007506.1:g.16416C= , LRG_193:g.16416C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366159.9:n.1758C=
ENST00000437813.8:c.*118C=	ENSP00000513672.1:n.*118C=
ENST00000440083.7:c.876C=	ENSP00000413224.3:p.Phe292=
ENST00000535038.2:n.839C=
ENST00000535958.2:c.*484C=	ENSP00000513673.1:n.*484C=
ENST00000698337.1:n.647C=
ENST00000698338.1:n.1071C=
ENST00000698339.1:c.*152C=	ENSP00000513670.1:n.*152C=
ENST00000698340.1:c.583C=	ENSP00000513671.1:p.Leu195=
ENST00000162749.7:c.657C= MANE Select	ENSP00000162749.2:p.Phe219=
ENST00000162749.6:c.657C=	ENSP00000162749.2:p.Phe219=
ENST00000534885.5:c.*134C=	ENSP00000441803.1:n.*134C=
ENST00000535038.1:n.468C=
ENST00000536717.5:n.561C=
ENST00000537842.5:n.261C=
ENST00000539372.5:c.657C=	ENSP00000442059.1:p.Phe219=
ENST00000540022.5:c.528C=	ENSP00000438343.1:p.Phe176=
ENST00000543359.5:n.69C=
ENST00000543995.5:c.*244C=	ENSP00000442405.1:n.*244C=
NM_001065.3:c.657C= , LRG_193t1:c.657C=	NP_001056.1:p.Phe219=
NM_001346091.1:c.333C=	NP_001333020.1:p.Phe111=
NM_001346092.1:c.198C=	NP_001333021.1:p.Phe66=
NR_144351.1:n.886C=
NM_001065.4:c.657C= MANE Select	NP_001056.1:p.Phe219=
NM_001346091.2:c.333C=	NP_001333020.1:p.Phe111=
NM_001346092.2:c.198C=	NP_001333021.1:p.Phe66=
NR_144351.2:n.845C=