Canonical Allele Identifier: CA1312515994
Gene: FRZB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.182838772_182838774delinsAGT , CM000664.2:g.182838772_182838774delinsAGT GRCh38
NC_000002.11:g.183703500_183703502delinsAGT , CM000664.1:g.183703500_183703502delinsAGT GRCh37
NC_000002.10:g.183411745_183411747delinsAGT NCBI36
NG_017197.1:g.32997_32999delinsACT

Transcript Alleles

HGVS Amino-acid Change
ENST00000295113.5:c.593-161_593-159delinsACT MANE Select ENSP00000295113.4:n.593-161_593-159delinsACT
ENST00000295113.4:c.593-161_593-159delinsACT ENSP00000295113.4:n.593-161_593-159delinsACT
NM_001463.3:c.593-161_593-159delinsACT NP_001454.2:n.593-161_593-159delinsACT
NM_001463.4:c.593-161_593-159delinsACT MANE Select NP_001454.2:n.593-161_593-159delinsACT