Canonical Allele Identifier: CA2617255597

Gene: TNFRSF1A

Linked Data

• gnomAD v4: 12-6333830-GC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6333834del , CM000674.2:g.6333834del	GRCh38
NC_000012.11:g.6443000del , CM000674.1:g.6443000del	GRCh37
NC_000012.10:g.6313261del	NCBI36
NG_007506.1:g.13265del , LRG_193:g.13265del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366159.9:n.262del
ENST00000437813.8:c.228del	ENSP00000513672.1:p.Gln77ArgfsTer?
ENST00000440083.7:c.228del	ENSP00000413224.3:p.Gln77ArgfsTer?
ENST00000535958.2:c.*55del	ENSP00000513673.1:n.*55del
ENST00000698339.1:c.228del	ENSP00000513670.1:p.Gln77ArgfsTer?
ENST00000698340.1:c.228del	ENSP00000513671.1:p.Gln77ArgfsTer?
ENST00000162749.7:c.228del MANE Select	ENSP00000162749.2:p.Gln77ArgfsTer?
ENST00000162749.6:c.228del	ENSP00000162749.2:p.Gln77ArgfsTer?
ENST00000366159.8:c.228del	ENSP00000380389.3:p.Gln77ArgfsTer?
ENST00000437813.7:n.189del
ENST00000440083.6:c.228del	ENSP00000413224.2:p.Gln77ArgfsTer?
ENST00000534885.5:c.74del	ENSP00000441803.1:p.Gly25AlafsTer9
ENST00000535958.1:n.474del
ENST00000536194.1:c.201del	ENSP00000442919.1:p.Gln68ArgfsTer?
ENST00000539372.5:c.228del	ENSP00000442059.1:p.Gln77ArgfsTer?
ENST00000540022.5:c.193+260del	ENSP00000438343.1:n.193+260del
ENST00000543048.5:c.214+14del	ENSP00000439981.1:n.214+14del
ENST00000543995.5:c.193+260del	ENSP00000442405.1:n.193+260del
NM_001065.3:c.228del , LRG_193t1:c.228del	NP_001056.1:p.Gln77ArgfsTer?
NM_001346091.1:c.-97del	NP_001333020.1:n.-97del
NM_001346092.1:c.-350del	NP_001333021.1:n.-350del
NR_144351.1:n.531del
NM_001065.4:c.228del MANE Select	NP_001056.1:p.Gln77ArgfsTer?
NM_001346091.2:c.-97del	NP_001333020.1:n.-97del
NM_001346092.2:c.-350del	NP_001333021.1:n.-350del
NR_144351.2:n.490del