Canonical Allele Identifier: CA2014024145

Gene: TNFRSF1A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6330815G= , CM000674.2:g.6330815G=	GRCh38
NC_000012.11:g.6439981G= , CM000674.1:g.6439981G=	GRCh37
NC_000012.10:g.6310242G=	NCBI36
NG_007506.1:g.16281C= , LRG_193:g.16281C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366159.9:n.1726+38C=
ENST00000437813.8:c.*86+38C=	ENSP00000513672.1:n.*86+38C=
ENST00000440083.7:c.844+38C=	ENSP00000413224.3:n.844+38C=
ENST00000535038.2:n.807+38C=
ENST00000535958.2:c.*452+38C=	ENSP00000513673.1:n.*452+38C=
ENST00000698337.1:n.512C=
ENST00000698338.1:n.936C=
ENST00000698339.1:c.*120+38C=	ENSP00000513670.1:n.*120+38C=
ENST00000698340.1:c.552-104C=	ENSP00000513671.1:n.552-104C=
ENST00000162749.7:c.625+38C= MANE Select	ENSP00000162749.2:n.625+38C=
ENST00000162749.6:c.625+38C=	ENSP00000162749.2:n.625+38C=
ENST00000534885.5:c.*102+38C=	ENSP00000441803.1:n.*102+38C=
ENST00000535038.1:n.333C=
ENST00000536717.5:n.529+38C=
ENST00000537842.5:n.229+38C=
ENST00000539372.5:c.625+38C=	ENSP00000442059.1:n.625+38C=
ENST00000540022.5:c.496+38C=	ENSP00000438343.1:n.496+38C=
ENST00000543359.5:n.38-104C=
ENST00000543995.5:c.*212+38C=	ENSP00000442405.1:n.*212+38C=
NM_001065.3:c.625+38C= , LRG_193t1:c.625+38C=	NP_001056.1:n.625+38C=
NM_001346091.1:c.301+38C=	NP_001333020.1:n.301+38C=
NM_001346092.1:c.166+38C=	NP_001333021.1:n.166+38C=
NR_144351.1:n.855-104C=
NM_001065.4:c.625+38C= MANE Select	NP_001056.1:n.625+38C=
NM_001346091.2:c.301+38C=	NP_001333020.1:n.301+38C=
NM_001346092.2:c.166+38C=	NP_001333021.1:n.166+38C=
NR_144351.2:n.814-104C=