Canonical Allele Identifier: CA6405561

Gene: TNFRSF1A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6333455C>T , CM000674.2:g.6333455C>T	GRCh38
NC_000012.11:g.6442621C>T , CM000674.1:g.6442621C>T	GRCh37
NC_000012.10:g.6312882C>T	NCBI36
NG_007506.1:g.13641G>A , LRG_193:g.13641G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001065.4:c.384G>A MANE Select	NP_001056.1:p.Arg128=
ENST00000162749.7:c.384G>A MANE Select	ENSP00000162749.2:p.Arg128=
NM_001065.3:c.384G>A , LRG_193t1:c.384G>A	NP_001056.1:p.Arg128=
NM_001346091.1:c.60G>A	NP_001333020.1:p.Arg20=
NM_001346091.2:c.60G>A	NP_001333020.1:p.Arg20=
NM_001346092.1:c.-194G>A	NP_001333021.1:n.-194G>A
NM_001346092.2:c.-194G>A	NP_001333021.1:n.-194G>A
NR_144351.1:n.687G>A
NR_144351.2:n.646G>A
ENST00000162749.6:c.384G>A	ENSP00000162749.2:p.Arg128=
ENST00000366159.8:c.384G>A	ENSP00000380389.3:p.Arg128=
ENST00000366159.9:n.418G>A
ENST00000437813.7:n.345G>A
ENST00000437813.8:c.384G>A	ENSP00000513672.1:p.Arg128=
ENST00000440083.6:c.384G>A	ENSP00000413224.2:p.Arg128=
ENST00000440083.7:c.384G>A	ENSP00000413224.3:p.Arg128=
ENST00000534885.5:c.230G>A	ENSP00000441803.1:p.Gly77Glu
ENST00000535958.2:c.*211G>A	ENSP00000513673.1:n.*211G>A
ENST00000539372.5:c.384G>A	ENSP00000442059.1:p.Arg128=
ENST00000540022.5:c.255G>A	ENSP00000438343.1:p.Arg85=
ENST00000543048.5:c.215-4G>A	ENSP00000439981.1:n.215-4G>A
ENST00000543995.5:c.194-4G>A	ENSP00000442405.1:n.194-4G>A
ENST00000698339.1:c.384G>A	ENSP00000513670.1:p.Arg128=
ENST00000698340.1:c.384G>A	ENSP00000513671.1:p.Arg128=