Canonical Allele Identifier: CA2546636291
Gene: TNFRSF11B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.118939443_118939444insT , CM000670.2:g.118939443_118939444insT GRCh38
NC_000008.10:g.119951682_119951683insT , CM000670.1:g.119951682_119951683insT GRCh37
NC_000008.9:g.120020863_120020864insT NCBI36
NG_012202.1:g.17701_17702insA

Transcript Alleles

HGVS Amino-acid change
ENST00000297350.9:c.31-6144_31-6143insA MANE Select ENSP00000297350.4:n.31-6144_31-6143insA
ENST00000297350.8:c.31-6144_31-6143insA ENSP00000297350.4:n.31-6144_31-6143insA
ENST00000517352.1:c.31-6144_31-6143insA ENSP00000427924.1:n.31-6144_31-6143insA
NM_002546.3:c.31-6144_31-6143insA NP_002537.3:n.31-6144_31-6143insA
NM_002546.4:c.31-6144_31-6143insA MANE Select NP_002537.3:n.31-6144_31-6143insA