Canonical Allele Identifier: CA2014024232

Gene: TNFRSF1A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6330874C= , CM000674.2:g.6330874C=	GRCh38
NC_000012.11:g.6440040C= , CM000674.1:g.6440040C=	GRCh37
NC_000012.10:g.6310301C=	NCBI36
NG_007506.1:g.16222G= , LRG_193:g.16222G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366159.9:n.1705G=
ENST00000437813.8:c.*65G=	ENSP00000513672.1:n.*65G=
ENST00000440083.7:c.823G=	ENSP00000413224.3:p.Val275=
ENST00000535038.2:n.786G=
ENST00000535958.2:c.*431G=	ENSP00000513673.1:n.*431G=
ENST00000698337.1:n.453G=
ENST00000698338.1:n.877G=
ENST00000698339.1:c.*99G=	ENSP00000513670.1:n.*99G=
ENST00000698340.1:c.552-163G=	ENSP00000513671.1:n.552-163G=
ENST00000162749.7:c.604G= MANE Select	ENSP00000162749.2:p.Val202=
ENST00000162749.6:c.604G=	ENSP00000162749.2:p.Val202=
ENST00000534885.5:c.*81G=	ENSP00000441803.1:n.*81G=
ENST00000535038.1:n.274G=
ENST00000536717.5:n.508G=
ENST00000537842.5:n.208G=
ENST00000539372.5:c.604G=	ENSP00000442059.1:p.Val202=
ENST00000540022.5:c.475G=	ENSP00000438343.1:p.Val159=
ENST00000543359.5:n.38-163G=
ENST00000543995.5:c.*191G=	ENSP00000442405.1:n.*191G=
NM_001065.3:c.604G= , LRG_193t1:c.604G=	NP_001056.1:p.Val202=
NM_001346091.1:c.280G=	NP_001333020.1:p.Val94=
NM_001346092.1:c.145G=	NP_001333021.1:p.Val49=
NR_144351.1:n.855-163G=
NM_001065.4:c.604G= MANE Select	NP_001056.1:p.Val202=
NM_001346091.2:c.280G=	NP_001333020.1:p.Val94=
NM_001346092.2:c.145G=	NP_001333021.1:p.Val49=
NR_144351.2:n.814-163G=