Canonical Allele Identifier: CA1312515975
Gene: FRZB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.182838724_182838725delinsCA , CM000664.2:g.182838724_182838725delinsCA GRCh38
NC_000002.11:g.183703452_183703453delinsCA , CM000664.1:g.183703452_183703453delinsCA GRCh37
NC_000002.10:g.183411697_183411698delinsCA NCBI36
NG_017197.1:g.33046_33047delinsTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000295113.5:c.593-112_593-111delinsTG MANE Select ENSP00000295113.4:n.593-112_593-111delinsTG
ENST00000295113.4:c.593-112_593-111delinsTG ENSP00000295113.4:n.593-112_593-111delinsTG
NM_001463.3:c.593-112_593-111delinsTG NP_001454.2:n.593-112_593-111delinsTG
NM_001463.4:c.593-112_593-111delinsTG MANE Select NP_001454.2:n.593-112_593-111delinsTG