Canonical Allele Identifier: CA2617243514

Gene: TNFRSF1A

Linked Data

• gnomAD v4: 12-6341696-GC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6341701del , CM000674.2:g.6341701del	GRCh38
NC_000012.11:g.6450867del , CM000674.1:g.6450867del	GRCh37
NC_000012.10:g.6321128del	NCBI36
NG_007506.1:g.5399del , LRG_193:g.5399del

Transcript Alleles

HGVS	Amino-acid change
ENST00000366159.9:n.73+79del
ENST00000437813.8:c.39+79del	ENSP00000513672.1:n.39+79del
ENST00000440083.7:c.39+79del	ENSP00000413224.3:n.39+79del
ENST00000535958.2:c.39+79del	ENSP00000513673.1:n.39+79del
ENST00000698339.1:c.39+79del	ENSP00000513670.1:n.39+79del
ENST00000698340.1:c.39+79del	ENSP00000513671.1:n.39+79del
ENST00000162749.7:c.39+79del MANE Select	ENSP00000162749.2:n.39+79del
ENST00000162749.6:c.39+79del	ENSP00000162749.2:n.39+79del
ENST00000366159.8:c.39+79del	ENSP00000380389.3:n.39+79del
ENST00000440083.6:c.39+79del	ENSP00000413224.2:n.39+79del
ENST00000534885.5:c.39+79del	ENSP00000441803.1:n.39+79del
ENST00000535958.1:n.260+79del
ENST00000536194.1:c.39+79del	ENSP00000442919.1:n.39+79del
ENST00000538363.1:n.229+79del
ENST00000539372.5:c.39+79del	ENSP00000442059.1:n.39+79del
ENST00000540022.5:c.39+79del	ENSP00000438343.1:n.39+79del
ENST00000543048.5:c.39+79del	ENSP00000439981.1:n.39+79del
ENST00000543995.5:c.39+79del	ENSP00000442405.1:n.39+79del
NM_001065.3:c.39+79del , LRG_193t1:c.39+79del	NP_001056.1:n.39+79del
NM_001346091.1:c.-132+79del	NP_001333020.1:n.-132+79del
NM_001346092.1:c.-539+79del	NP_001333021.1:n.-539+79del
NR_144351.1:n.342+79del
NM_001065.4:c.39+79del MANE Select	NP_001056.1:n.39+79del
NM_001346091.2:c.-132+79del	NP_001333020.1:n.-132+79del
NM_001346092.2:c.-539+79del	NP_001333021.1:n.-539+79del
NR_144351.2:n.301+79del