Canonical Allele Identifier: CA645595462

Gene: TNFRSF1A

Linked Data

• gnomAD v4: 12-6333066-CACTT-C
• COSMIC: COSM4734893

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6333070_6333073del , CM000674.2:g.6333070_6333073del	GRCh38
NC_000012.11:g.6442236_6442239del , CM000674.1:g.6442236_6442239del	GRCh37
NC_000012.10:g.6312497_6312500del	NCBI36
NG_007506.1:g.14026_14029del , LRG_193:g.14026_14029del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366159.9:n.584_585+2del
ENST00000437813.8:c.550_551+2del
ENST00000440083.7:c.769_770+2del
ENST00000535958.2:c.*377_*378+2del
ENST00000698339.1:c.550_551+2del
ENST00000698340.1:c.550_551+2del
ENST00000162749.7:c.550_551+2del
ENST00000162749.6:c.550_551+2del
ENST00000366159.8:c.550_551+2del
ENST00000437813.7:n.511_512+2del
ENST00000534885.5:c.*27_*28+2del
ENST00000537842.5:n.154_155+2del
ENST00000539372.5:c.550_551+2del
ENST00000540022.5:c.421_422+2del
ENST00000543048.5:c.*161_*164del	ENSP00000439981.1:n.*161_*164del
ENST00000543359.5:n.36_37+2del
ENST00000543995.5:c.*137_*138+2del
NM_001065.3:c.550_551+2del , LRG_193t1:c.550_551+2del
NM_001346091.1:c.226_227+2del
NM_001346092.1:c.-28_-27+2del
NR_144351.1:n.853_854+2del
NM_001065.4:c.550_551+2del
NM_001346091.2:c.226_227+2del
NM_001346092.2:c.-28_-27+2del
NR_144351.2:n.812_813+2del