Canonical Allele Identifier: CA2753437686
Gene: FRZB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.182838279_182838286del , CM000664.2:g.182838279_182838286del GRCh38
NC_000002.11:g.183703007_183703014del , CM000664.1:g.183703007_183703014del GRCh37
NC_000002.10:g.183411252_183411259del NCBI36
NG_017197.1:g.33485_33492del

Transcript Alleles

HGVS Amino-acid Change
ENST00000295113.5:c.797+123_797+130del MANE Select ENSP00000295113.4:n.797+123_797+130del
ENST00000295113.4:c.797+123_797+130del ENSP00000295113.4:n.797+123_797+130del
NM_001463.3:c.797+123_797+130del NP_001454.2:n.797+123_797+130del
NM_001463.4:c.797+123_797+130del MANE Select NP_001454.2:n.797+123_797+130del