Canonical Allele Identifier: CA2753437692
Gene: FRZB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.182838678_182838679insAAAAAAAA , CM000664.2:g.182838678_182838679insAAAAAAAA GRCh38
NC_000002.11:g.183703406_183703407insAAAAAAAA , CM000664.1:g.183703406_183703407insAAAAAAAA GRCh37
NC_000002.10:g.183411651_183411652insAAAAAAAA NCBI36
NG_017197.1:g.33099_33100insTTTTTTTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000295113.5:c.593-59_593-58insTTTTTTTT MANE Select ENSP00000295113.4:n.593-59_593-58insTTTTTTTT
ENST00000295113.4:c.593-59_593-58insTTTTTTTT ENSP00000295113.4:n.593-59_593-58insTTTTTTTT
NM_001463.3:c.593-59_593-58insTTTTTTTT NP_001454.2:n.593-59_593-58insTTTTTTTT
NM_001463.4:c.593-59_593-58insTTTTTTTT MANE Select NP_001454.2:n.593-59_593-58insTTTTTTTT