Canonical Allele Identifier: CA1770755922

Gene: TNFRSF10A

Linked Data

• dbSNP Id: rs1801100012

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.23212085dup , CM000670.2:g.23212085dup	GRCh38
NC_000008.10:g.23069598dup , CM000670.1:g.23069598dup	GRCh37
NC_000008.9:g.23125543dup	NCBI36
NG_032107.1:g.18083dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000221132.8:c.403+31dup MANE Select	ENSP00000221132.3:n.403+31dup
ENST00000221132.7:c.403+31dup	ENSP00000221132.3:n.403+31dup
ENST00000524158.5:c.-204+31dup	ENSP00000428884.1:n.-204+31dup
ENST00000613472.1:c.32-9426dup	ENSP00000480778.1:n.32-9426dup
NM_003844.3:c.403+31dup	NP_003835.3:n.403+31dup
NM_003844.4:c.403+31dup MANE Select	NP_003835.3:n.403+31dup