Canonical Allele Identifier: CA580573868
Gene: TNFRSF10A HGNC NCBI

Linked Data

dbSNP Id: rs1351657480
gnomAD v2: 8-23069585-GAA-G
gnomAD v3: 8-23212072-GAA-G
gnomAD v4: 8-23212072-GAA-G
MyVariant Identifiers: chr8:g.23069586_23069587del (hg19) chr8:g.23212073_23212074del (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.23212075_23212076del , CM000670.2:g.23212075_23212076del GRCh38
NC_000008.10:g.23069588_23069589del , CM000670.1:g.23069588_23069589del GRCh37
NC_000008.9:g.23125533_23125534del NCBI36
NG_032107.1:g.18094_18095del

Transcript Alleles

HGVS Amino-acid Change
ENST00000221132.8:c.403+42_403+43del MANE Select ENSP00000221132.3:n.403+42_403+43del
ENST00000221132.7:c.403+42_403+43del ENSP00000221132.3:n.403+42_403+43del
ENST00000524158.5:c.-204+42_-204+43del ENSP00000428884.1:n.-204+42_-204+43del
ENST00000613472.1:c.32-9415_32-9414del ENSP00000480778.1:n.32-9415_32-9414del
NM_003844.3:c.403+42_403+43del NP_003835.3:n.403+42_403+43del
NM_003844.4:c.403+42_403+43del MANE Select NP_003835.3:n.403+42_403+43del
Search 100 bp 5'
Search 100 bp 3'