Canonical Allele Identifier: CA2653589339

Gene: CDH4

Linked Data

• gnomAD v4: 20-61928224-G-GATCT

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.61928229_61928232dup , CM000682.2:g.61928229_61928232dup	GRCh38
NC_000020.10:g.60503287_60503290dup , CM000682.1:g.60503287_60503290dup	GRCh37
NC_000020.9:g.59936682_59936685dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000614565.5:c.1811_1814dup MANE Select	ENSP00000484928.1:p.Ile606SerfsTer3
ENST00000543233.2:c.1589_1592dup	ENSP00000443301.1:p.Ile532SerfsTer3
ENST00000611855.4:c.1529_1532dup	ENSP00000480844.1:p.Ile512SerfsTer3
ENST00000614565.4:c.1811_1814dup	ENSP00000484928.1:p.Ile606SerfsTer3
NM_001252338.2:c.1700_1703dup	NP_001239267.1:p.Ile569SerfsTer3
NM_001252339.2:c.1589_1592dup	NP_001239268.1:p.Ile532SerfsTer3
NM_001794.4:c.1811_1814dup	NP_001785.2:p.Ile606SerfsTer3
NM_001794.5:c.1811_1814dup MANE Select	NP_001785.2:p.Ile606SerfsTer3
NM_001252339.3:c.1589_1592dup	NP_001239268.1:p.Ile532SerfsTer3