Canonical Allele Identifier: CA2662236438

Gene: FRZB

Linked Data

• gnomAD v4: 2-182838664-C-CTTTGCTTAT

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.182838664_182838665insTTTGCTTAT , CM000664.2:g.182838664_182838665insTTTGCTTAT	GRCh38
NC_000002.11:g.183703392_183703393insTTTGCTTAT , CM000664.1:g.183703392_183703393insTTTGCTTAT	GRCh37
NC_000002.10:g.183411637_183411638insTTTGCTTAT	NCBI36
NG_017197.1:g.33106_33107insATAAGCAAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295113.5:c.593-52_593-51insATAAGCAAA MANE Select	ENSP00000295113.4:n.593-52_593-51insATAAGCAAA
ENST00000295113.4:c.593-52_593-51insATAAGCAAA	ENSP00000295113.4:n.593-52_593-51insATAAGCAAA
NM_001463.3:c.593-52_593-51insATAAGCAAA	NP_001454.2:n.593-52_593-51insATAAGCAAA
NM_001463.4:c.593-52_593-51insATAAGCAAA MANE Select	NP_001454.2:n.593-52_593-51insATAAGCAAA