Canonical Allele Identifier: CA1814472644
Gene: TNFRSF11B HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.118934371_118934373delinsACT , CM000670.2:g.118934371_118934373delinsACT GRCh38
NC_000008.10:g.119946610_119946612delinsACT , CM000670.1:g.119946610_119946612delinsACT GRCh37
NC_000008.9:g.120015791_120015793delinsACT NCBI36
NG_012202.1:g.22772_22774delinsAGT

Transcript Alleles

HGVS Amino-acid change
ENST00000297350.9:c.31-1073_31-1071delinsAGT MANE Select ENSP00000297350.4:n.31-1073_31-1071delinsAGT
ENST00000297350.8:c.31-1073_31-1071delinsAGT ENSP00000297350.4:n.31-1073_31-1071delinsAGT
ENST00000517352.1:c.31-1073_31-1071delinsAGT ENSP00000427924.1:n.31-1073_31-1071delinsAGT
NM_002546.3:c.31-1073_31-1071delinsAGT NP_002537.3:n.31-1073_31-1071delinsAGT
NM_002546.4:c.31-1073_31-1071delinsAGT MANE Select NP_002537.3:n.31-1073_31-1071delinsAGT
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