Canonical Allele Identifier: CA1111806682

Gene: TNFRSF10A

Linked Data

• dbSNP Id: rs1801271061
• gnomAD v3: 8-23222494-T-TA
• gnomAD v4: 8-23222494-T-TA

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.23222499dup , CM000670.2:g.23222499dup	GRCh38
NC_000008.10:g.23080012dup , CM000670.1:g.23080012dup	GRCh37
NC_000008.9:g.23135957dup	NCBI36
NG_032107.1:g.7673dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000221132.8:c.306+2261dup MANE Select	ENSP00000221132.3:n.306+2261dup
ENST00000221132.7:c.306+2261dup	ENSP00000221132.3:n.306+2261dup
ENST00000524158.5:c.-301+1938dup	ENSP00000428884.1:n.-301+1938dup
ENST00000613472.1:c.31+2536dup	ENSP00000480778.1:n.31+2536dup
NM_003844.3:c.306+2261dup	NP_003835.3:n.306+2261dup
NM_003844.4:c.306+2261dup MANE Select	NP_003835.3:n.306+2261dup