Canonical Allele Identifier: CA658105962

Gene: CDH4

Linked Data

• COSMIC: COSN196238

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.61531922_61531947delinsAATC , CM000682.2:g.61531922_61531947delinsAATC	GRCh38
NC_000020.10:g.60106978_60107003delinsAATC , CM000682.1:g.60106978_60107003delinsAATC	GRCh37
NC_000020.9:g.59540373_59540398delinsAATC	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000614565.5:c.170-211641_170-211616delinsAATC MANE Select	ENSP00000484928.1:n.170-211641_170-211616delinsAATC
ENST00000614565.4:c.170-211641_170-211616delinsAATC	ENSP00000484928.1:n.170-211641_170-211616delinsAATC
NM_001252338.2:c.58+32430_58+32455delinsAATC	NP_001239267.1:n.58+32430_58+32455delinsAATC
NM_001794.4:c.170-211641_170-211616delinsAATC	NP_001785.2:n.170-211641_170-211616delinsAATC
NM_001794.5:c.170-211641_170-211616delinsAATC MANE Select	NP_001785.2:n.170-211641_170-211616delinsAATC