Canonical Allele Identifier: CA2014024108

Gene: TNFRSF1A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6330756G= , CM000674.2:g.6330756G=	GRCh38
NC_000012.11:g.6439922G= , CM000674.1:g.6439922G=	GRCh37
NC_000012.10:g.6310183G=	NCBI36
NG_007506.1:g.16340C= , LRG_193:g.16340C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366159.9:n.1727-45C=
ENST00000437813.8:c.*87-45C=	ENSP00000513672.1:n.*87-45C=
ENST00000440083.7:c.845-45C=	ENSP00000413224.3:n.845-45C=
ENST00000535038.2:n.808-45C=
ENST00000535958.2:c.*453-45C=	ENSP00000513673.1:n.*453-45C=
ENST00000698337.1:n.571C=
ENST00000698338.1:n.995C=
ENST00000698339.1:c.*121-45C=	ENSP00000513670.1:n.*121-45C=
ENST00000698340.1:c.552-45C=	ENSP00000513671.1:n.552-45C=
ENST00000162749.7:c.626-45C= MANE Select	ENSP00000162749.2:n.626-45C=
ENST00000162749.6:c.626-45C=	ENSP00000162749.2:n.626-45C=
ENST00000534885.5:c.*103-45C=	ENSP00000441803.1:n.*103-45C=
ENST00000535038.1:n.392C=
ENST00000536717.5:n.530-45C=
ENST00000537842.5:n.230-45C=
ENST00000539372.5:c.626-45C=	ENSP00000442059.1:n.626-45C=
ENST00000540022.5:c.497-45C=	ENSP00000438343.1:n.497-45C=
ENST00000543359.5:n.38-45C=
ENST00000543995.5:c.*213-45C=	ENSP00000442405.1:n.*213-45C=
NM_001065.3:c.626-45C= , LRG_193t1:c.626-45C=	NP_001056.1:n.626-45C=
NM_001346091.1:c.302-45C=	NP_001333020.1:n.302-45C=
NM_001346092.1:c.167-45C=	NP_001333021.1:n.167-45C=
NR_144351.1:n.855-45C=
NM_001065.4:c.626-45C= MANE Select	NP_001056.1:n.626-45C=
NM_001346091.2:c.302-45C=	NP_001333020.1:n.302-45C=
NM_001346092.2:c.167-45C=	NP_001333021.1:n.167-45C=
NR_144351.2:n.814-45C=