Canonical Allele Identifier: CA2617254169

Gene: TNFRSF1A

Linked Data

• gnomAD v4: 12-6333062-TACTC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6333066_6333069del , CM000674.2:g.6333066_6333069del	GRCh38
NC_000012.11:g.6442232_6442235del , CM000674.1:g.6442232_6442235del	GRCh37
NC_000012.10:g.6312493_6312496del	NCBI36
NG_007506.1:g.14030_14033del , LRG_193:g.14030_14033del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366159.9:n.585+3_585+6del
ENST00000437813.8:c.551+3_551+6del
ENST00000440083.7:c.770+3_770+6del
ENST00000535958.2:c.*378+3_*378+6del
ENST00000698339.1:c.551+3_551+6del
ENST00000698340.1:c.551+3_551+6del
ENST00000162749.7:c.551+3_551+6del
ENST00000162749.6:c.551+3_551+6del
ENST00000366159.8:c.551+3_551+6del
ENST00000437813.7:n.512+3_512+6del
ENST00000534885.5:c.*28+3_*28+6del
ENST00000537842.5:n.155+3_155+6del
ENST00000539372.5:c.551+3_551+6del
ENST00000540022.5:c.422+3_422+6del
ENST00000543359.5:n.37+3_37+6del
ENST00000543995.5:c.*138+3_*138+6del
NM_001065.3:c.551+3_551+6del , LRG_193t1:c.551+3_551+6del
NM_001346091.1:c.227+3_227+6del
NM_001346092.1:c.-27+3_-27+6del
NR_144351.1:n.854+3_854+6del
NM_001065.4:c.551+3_551+6del
NM_001346091.2:c.227+3_227+6del
NM_001346092.2:c.-27+3_-27+6del
NR_144351.2:n.813+3_813+6del