Canonical Allele Identifier: CA2617254331

Gene: TNFRSF1A

Linked Data

• gnomAD v4: 12-6333188-GCACCCC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6333195_6333200del , CM000674.2:g.6333195_6333200del	GRCh38
NC_000012.11:g.6442361_6442366del , CM000674.1:g.6442361_6442366del	GRCh37
NC_000012.10:g.6312622_6312627del	NCBI36
NG_007506.1:g.13902_13907del , LRG_193:g.13902_13907del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366159.9:n.507-47_507-42del
ENST00000437813.8:c.473-47_473-42del	ENSP00000513672.1:n.473-47_473-42del
ENST00000440083.7:c.645_650del	ENSP00000413224.3:p.Trp215_Gly216del
ENST00000535958.2:c.*300-47_*300-42del	ENSP00000513673.1:n.*300-47_*300-42del
ENST00000698339.1:c.473-47_473-42del	ENSP00000513670.1:n.473-47_473-42del
ENST00000698340.1:c.473-47_473-42del	ENSP00000513671.1:n.473-47_473-42del
ENST00000162749.7:c.473-47_473-42del MANE Select	ENSP00000162749.2:n.473-47_473-42del
ENST00000162749.6:c.473-47_473-42del	ENSP00000162749.2:n.473-47_473-42del
ENST00000366159.8:c.473-47_473-42del	ENSP00000380389.3:n.473-47_473-42del
ENST00000437813.7:n.434-47_434-42del
ENST00000440083.6:c.645_650del	ENSP00000413224.2:p.Trp215_Gly216del
ENST00000534885.5:c.319-47_319-42del	ENSP00000441803.1:n.319-47_319-42del
ENST00000537842.5:n.77-47_77-42del
ENST00000539372.5:c.473-47_473-42del	ENSP00000442059.1:n.473-47_473-42del
ENST00000540022.5:c.344-47_344-42del	ENSP00000438343.1:n.344-47_344-42del
ENST00000543048.5:c.*84-47_*84-42del	ENSP00000439981.1:n.*84-47_*84-42del
ENST00000543995.5:c.*60-47_*60-42del	ENSP00000442405.1:n.*60-47_*60-42del
NM_001065.3:c.473-47_473-42del , LRG_193t1:c.473-47_473-42del	NP_001056.1:n.473-47_473-42del
NM_001346091.1:c.149-47_149-42del	NP_001333020.1:n.149-47_149-42del
NM_001346092.1:c.-105-47_-105-42del	NP_001333021.1:n.-105-47_-105-42del
NR_144351.1:n.776-47_776-42del
NM_001065.4:c.473-47_473-42del MANE Select	NP_001056.1:n.473-47_473-42del
NM_001346091.2:c.149-47_149-42del	NP_001333020.1:n.149-47_149-42del
NM_001346092.2:c.-105-47_-105-42del	NP_001333021.1:n.-105-47_-105-42del
NR_144351.2:n.735-47_735-42del