Canonical Allele Identifier: CA2617254392

Gene: TNFRSF1A

Linked Data

• gnomAD v4: 12-6333202-CAGGACAGAGGAA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6333203_6333214del , CM000674.2:g.6333203_6333214del	GRCh38
NC_000012.11:g.6442369_6442380del , CM000674.1:g.6442369_6442380del	GRCh37
NC_000012.10:g.6312630_6312641del	NCBI36
NG_007506.1:g.13882_13893del , LRG_193:g.13882_13893del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366159.9:n.507-67_507-56del
ENST00000437813.8:c.473-67_473-56del	ENSP00000513672.1:n.473-67_473-56del
ENST00000440083.7:c.625_636del	ENSP00000413224.3:p.Phe209_Pro212del
ENST00000535958.2:c.*300-67_*300-56del	ENSP00000513673.1:n.*300-67_*300-56del
ENST00000698339.1:c.473-67_473-56del	ENSP00000513670.1:n.473-67_473-56del
ENST00000698340.1:c.473-67_473-56del	ENSP00000513671.1:n.473-67_473-56del
ENST00000162749.7:c.473-67_473-56del MANE Select	ENSP00000162749.2:n.473-67_473-56del
ENST00000162749.6:c.473-67_473-56del	ENSP00000162749.2:n.473-67_473-56del
ENST00000366159.8:c.473-67_473-56del	ENSP00000380389.3:n.473-67_473-56del
ENST00000437813.7:n.434-67_434-56del
ENST00000440083.6:c.625_636del	ENSP00000413224.2:p.Phe209_Pro212del
ENST00000534885.5:c.319-67_319-56del	ENSP00000441803.1:n.319-67_319-56del
ENST00000537842.5:n.77-67_77-56del
ENST00000539372.5:c.473-67_473-56del	ENSP00000442059.1:n.473-67_473-56del
ENST00000540022.5:c.344-67_344-56del	ENSP00000438343.1:n.344-67_344-56del
ENST00000543048.5:c.*84-67_*84-56del	ENSP00000439981.1:n.*84-67_*84-56del
ENST00000543995.5:c.*60-67_*60-56del	ENSP00000442405.1:n.*60-67_*60-56del
NM_001065.3:c.473-67_473-56del , LRG_193t1:c.473-67_473-56del	NP_001056.1:n.473-67_473-56del
NM_001346091.1:c.149-67_149-56del	NP_001333020.1:n.149-67_149-56del
NM_001346092.1:c.-105-67_-105-56del	NP_001333021.1:n.-105-67_-105-56del
NR_144351.1:n.776-67_776-56del
NM_001065.4:c.473-67_473-56del MANE Select	NP_001056.1:n.473-67_473-56del
NM_001346091.2:c.149-67_149-56del	NP_001333020.1:n.149-67_149-56del
NM_001346092.2:c.-105-67_-105-56del	NP_001333021.1:n.-105-67_-105-56del
NR_144351.2:n.735-67_735-56del