Canonical Allele Identifier: CA2014025884

Gene: TNFRSF1A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6333125C= , CM000674.2:g.6333125C=	GRCh38
NC_000012.11:g.6442291C= , CM000674.1:g.6442291C=	GRCh37
NC_000012.10:g.6312552C=	NCBI36
NG_007506.1:g.13971G= , LRG_193:g.13971G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366159.9:n.529G=
ENST00000437813.8:c.495G=	ENSP00000513672.1:p.Val165=
ENST00000440083.7:c.714G=	ENSP00000413224.3:p.Val238=
ENST00000535958.2:c.*322G=	ENSP00000513673.1:n.*322G=
ENST00000698339.1:c.495G=	ENSP00000513670.1:p.Val165=
ENST00000698340.1:c.495G=	ENSP00000513671.1:p.Val165=
ENST00000162749.7:c.495G= MANE Select	ENSP00000162749.2:p.Val165=
ENST00000162749.6:c.495G=	ENSP00000162749.2:p.Val165=
ENST00000366159.8:c.495G=	ENSP00000380389.3:p.Val165=
ENST00000437813.7:n.456G=
ENST00000440083.6:c.714G=	ENSP00000413224.2:p.Val238=
ENST00000534885.5:c.341G=	ENSP00000441803.1:p.Cys114=
ENST00000537842.5:n.99G=
ENST00000539372.5:c.495G=	ENSP00000442059.1:p.Val165=
ENST00000540022.5:c.366G=	ENSP00000438343.1:p.Val122=
ENST00000543048.5:c.*106G=	ENSP00000439981.1:n.*106G=
ENST00000543995.5:c.*82G=	ENSP00000442405.1:n.*82G=
NM_001065.3:c.495G= , LRG_193t1:c.495G=	NP_001056.1:p.Val165=
NM_001346091.1:c.171G=	NP_001333020.1:p.Val57=
NM_001346092.1:c.-83G=	NP_001333021.1:n.-83G=
NR_144351.1:n.798G=
NM_001065.4:c.495G= MANE Select	NP_001056.1:p.Val165=
NM_001346091.2:c.171G=	NP_001333020.1:p.Val57=
NM_001346092.2:c.-83G=	NP_001333021.1:n.-83G=
NR_144351.2:n.757G=