Canonical Allele Identifier: CA2014024246

Gene: TNFRSF1A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6330893G= , CM000674.2:g.6330893G=	GRCh38
NC_000012.11:g.6440059G= , CM000674.1:g.6440059G=	GRCh37
NC_000012.10:g.6310320G=	NCBI36
NG_007506.1:g.16203C= , LRG_193:g.16203C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366159.9:n.1686C=
ENST00000437813.8:c.*46C=	ENSP00000513672.1:n.*46C=
ENST00000440083.7:c.804C=	ENSP00000413224.3:p.Cys268=
ENST00000535038.2:n.767C=
ENST00000535958.2:c.*412C=	ENSP00000513673.1:n.*412C=
ENST00000698337.1:n.434C=
ENST00000698338.1:n.858C=
ENST00000698339.1:c.*80C=	ENSP00000513670.1:n.*80C=
ENST00000698340.1:c.552-182C=	ENSP00000513671.1:n.552-182C=
ENST00000162749.7:c.585C= MANE Select	ENSP00000162749.2:p.Cys195=
ENST00000162749.6:c.585C=	ENSP00000162749.2:p.Cys195=
ENST00000534885.5:c.*62C=	ENSP00000441803.1:n.*62C=
ENST00000535038.1:n.255C=
ENST00000536717.5:n.489C=
ENST00000537842.5:n.189C=
ENST00000539372.5:c.585C=	ENSP00000442059.1:p.Cys195=
ENST00000540022.5:c.456C=	ENSP00000438343.1:p.Cys152=
ENST00000543359.5:n.38-182C=
ENST00000543995.5:c.*172C=	ENSP00000442405.1:n.*172C=
NM_001065.3:c.585C= , LRG_193t1:c.585C=	NP_001056.1:p.Cys195=
NM_001346091.1:c.261C=	NP_001333020.1:p.Cys87=
NM_001346092.1:c.126C=	NP_001333021.1:p.Cys42=
NR_144351.1:n.855-182C=
NM_001065.4:c.585C= MANE Select	NP_001056.1:p.Cys195=
NM_001346091.2:c.261C=	NP_001333020.1:p.Cys87=
NM_001346092.2:c.126C=	NP_001333021.1:p.Cys42=
NR_144351.2:n.814-182C=