Canonical Allele Identifier: CA2014026053

Gene: TNFRSF1A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6333404A= , CM000674.2:g.6333404A=	GRCh38
NC_000012.11:g.6442570A= , CM000674.1:g.6442570A=	GRCh37
NC_000012.10:g.6312831A=	NCBI36
NG_007506.1:g.13692T= , LRG_193:g.13692T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366159.9:n.469T=
ENST00000437813.8:c.435T=	ENSP00000513672.1:p.Asn145=
ENST00000440083.7:c.435T=	ENSP00000413224.3:p.Asn145=
ENST00000535958.2:c.*262T=	ENSP00000513673.1:n.*262T=
ENST00000698339.1:c.435T=	ENSP00000513670.1:p.Asn145=
ENST00000698340.1:c.435T=	ENSP00000513671.1:p.Asn145=
ENST00000162749.7:c.435T= MANE Select	ENSP00000162749.2:p.Asn145=
ENST00000162749.6:c.435T=	ENSP00000162749.2:p.Asn145=
ENST00000366159.8:c.435T=	ENSP00000380389.3:p.Asn145=
ENST00000437813.7:n.396T=
ENST00000440083.6:c.435T=	ENSP00000413224.2:p.Asn145=
ENST00000534885.5:c.281T=	ENSP00000441803.1:p.Ile94=
ENST00000537842.5:n.39T=
ENST00000539372.5:c.435T=	ENSP00000442059.1:p.Asn145=
ENST00000540022.5:c.306T=	ENSP00000438343.1:p.Asn102=
ENST00000543048.5:c.*46T=	ENSP00000439981.1:n.*46T=
ENST00000543995.5:c.*22T=	ENSP00000442405.1:n.*22T=
NM_001065.3:c.435T= , LRG_193t1:c.435T=	NP_001056.1:p.Asn145=
NM_001346091.1:c.111T=	NP_001333020.1:p.Asn37=
NM_001346092.1:c.-143T=	NP_001333021.1:n.-143T=
NR_144351.1:n.738T=
NM_001065.4:c.435T= MANE Select	NP_001056.1:p.Asn145=
NM_001346091.2:c.111T=	NP_001333020.1:p.Asn37=
NM_001346092.2:c.-143T=	NP_001333021.1:n.-143T=
NR_144351.2:n.697T=