Canonical Allele Identifier: CA14802081

Gene: CDH4

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.61806743G>A , CM000682.2:g.61806743G>A	GRCh38
NC_000020.10:g.60381799G>A , CM000682.1:g.60381799G>A	GRCh37
NC_000020.9:g.59815194G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000614565.5:c.576+33561G>A MANE Select	ENSP00000484928.1:n.576+33561G>A
ENST00000543233.2:c.354+33561G>A	ENSP00000443301.1:n.354+33561G>A
ENST00000611855.4:c.294+33561G>A	ENSP00000480844.1:n.294+33561G>A
ENST00000614565.4:c.576+33561G>A	ENSP00000484928.1:n.576+33561G>A
NM_001252338.2:c.465+33561G>A	NP_001239267.1:n.465+33561G>A
NM_001252339.2:c.354+33561G>A	NP_001239268.1:n.354+33561G>A
NM_001794.4:c.576+33561G>A	NP_001785.2:n.576+33561G>A
NM_001794.5:c.576+33561G>A MANE Select	NP_001785.2:n.576+33561G>A
NM_001252339.3:c.354+33561G>A	NP_001239268.1:n.354+33561G>A