Canonical Allele Identifier: CA2753437697
Gene: FRZB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.182838778_182838779insTGTTTTATGTCACACACTACA , CM000664.2:g.182838778_182838779insTGTTTTATGTCACACACTACA GRCh38
NC_000002.11:g.183703506_183703507insTGTTTTATGTCACACACTACA , CM000664.1:g.183703506_183703507insTGTTTTATGTCACACACTACA GRCh37
NC_000002.10:g.183411751_183411752insTGTTTTATGTCACACACTACA NCBI36
NG_017197.1:g.32992_32993insTGTAGTGTGTGACATAAAACA

Transcript Alleles

HGVS Amino-acid Change
ENST00000295113.5:c.593-166_593-165insTGTAGTGTGTGACATAAAACA MANE Select ENSP00000295113.4:n.593-166_593-165insTGTAGTGTGTGACATAAAACA
ENST00000295113.4:c.593-166_593-165insTGTAGTGTGTGACATAAAACA ENSP00000295113.4:n.593-166_593-165insTGTAGTGTGTGACATAAAACA
NM_001463.3:c.593-166_593-165insTGTAGTGTGTGACATAAAACA NP_001454.2:n.593-166_593-165insTGTAGTGTGTGACATAAAACA
NM_001463.4:c.593-166_593-165insTGTAGTGTGTGACATAAAACA MANE Select NP_001454.2:n.593-166_593-165insTGTAGTGTGTGACATAAAACA