Canonical Allele Identifier: CA2662236409

Gene: FRZB

Linked Data

• gnomAD v4: 2-182838372-CAAAGT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.182838374_182838378del , CM000664.2:g.182838374_182838378del	GRCh38
NC_000002.11:g.183703102_183703106del , CM000664.1:g.183703102_183703106del	GRCh37
NC_000002.10:g.183411347_183411351del	NCBI36
NG_017197.1:g.33394_33398del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295113.5:c.797+32_797+36del MANE Select	ENSP00000295113.4:n.797+32_797+36del
ENST00000295113.4:c.797+32_797+36del	ENSP00000295113.4:n.797+32_797+36del
NM_001463.3:c.797+32_797+36del	NP_001454.2:n.797+32_797+36del
NM_001463.4:c.797+32_797+36del MANE Select	NP_001454.2:n.797+32_797+36del