Canonical Allele Identifier: CA2617249113

Gene: TNFRSF1A

Linked Data

• gnomAD v4: 12-6329809-CT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6329810del , CM000674.2:g.6329810del	GRCh38
NC_000012.11:g.6438976del , CM000674.1:g.6438976del	GRCh37
NC_000012.10:g.6309237del	NCBI36
NG_007506.1:g.17286del , LRG_193:g.17286del

Transcript Alleles

HGVS	Amino-acid change
ENST00000366159.9:n.2126del
ENST00000437813.8:c.*486del	ENSP00000513672.1:n.*486del
ENST00000440083.7:c.1244del	ENSP00000413224.3:p.Glu415GlyfsTer10
ENST00000535958.2:c.*852del	ENSP00000513673.1:n.*852del
ENST00000698337.1:n.986del
ENST00000698338.1:n.1639del
ENST00000698339.1:c.*520del	ENSP00000513670.1:n.*520del
ENST00000698340.1:c.*264del	ENSP00000513671.1:n.*264del
ENST00000162749.7:c.1025del MANE Select	ENSP00000162749.2:p.Glu342GlyfsTer10
ENST00000162749.6:c.1025del	ENSP00000162749.2:p.Glu342GlyfsTer10
ENST00000534885.5:c.*502del	ENSP00000441803.1:n.*502del
ENST00000536717.5:n.929del
ENST00000540022.5:c.896del	ENSP00000438343.1:p.Glu299GlyfsTer10
ENST00000543359.5:n.437del
ENST00000543995.5:c.*612del	ENSP00000442405.1:n.*612del
NM_001065.3:c.1025del , LRG_193t1:c.1025del	NP_001056.1:p.Glu342GlyfsTer10
NM_001346091.1:c.701del	NP_001333020.1:p.Glu234GlyfsTer10
NM_001346092.1:c.566del	NP_001333021.1:p.Glu189GlyfsTer10
NR_144351.1:n.1254del
NM_001065.4:c.1025del MANE Select	NP_001056.1:p.Glu342GlyfsTer10
NM_001346091.2:c.701del	NP_001333020.1:p.Glu234GlyfsTer10
NM_001346092.2:c.566del	NP_001333021.1:p.Glu189GlyfsTer10
NR_144351.2:n.1213del