Canonical Allele Identifier: CA1312515948

Gene: FRZB

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.182838663_182838665delinsACC , CM000664.2:g.182838663_182838665delinsACC	GRCh38
NC_000002.11:g.183703391_183703393delinsACC , CM000664.1:g.183703391_183703393delinsACC	GRCh37
NC_000002.10:g.183411636_183411638delinsACC	NCBI36
NG_017197.1:g.33106_33108delinsGGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295113.5:c.593-52_593-50delinsGGT MANE Select	ENSP00000295113.4:n.593-52_593-50delinsGGT
ENST00000295113.4:c.593-52_593-50delinsGGT	ENSP00000295113.4:n.593-52_593-50delinsGGT
NM_001463.3:c.593-52_593-50delinsGGT	NP_001454.2:n.593-52_593-50delinsGGT
NM_001463.4:c.593-52_593-50delinsGGT MANE Select	NP_001454.2:n.593-52_593-50delinsGGT