Canonical Allele Identifier: CA14764297

Gene: CDH4

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.61668355G>A , CM000682.2:g.61668355G>A	GRCh38
NC_000020.10:g.60243411G>A , CM000682.1:g.60243411G>A	GRCh37
NC_000020.9:g.59676806G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000614565.5:c.170-75208G>A MANE Select	ENSP00000484928.1:n.170-75208G>A
ENST00000543233.2:c.-54+68366G>A	ENSP00000443301.1:n.-54+68366G>A
ENST00000611855.4:c.50-75208G>A	ENSP00000480844.1:n.50-75208G>A
ENST00000614565.4:c.170-75208G>A	ENSP00000484928.1:n.170-75208G>A
NM_001252338.2:c.59-75208G>A	NP_001239267.1:n.59-75208G>A
NM_001252339.2:c.-54+68366G>A	NP_001239268.1:n.-54+68366G>A
NM_001794.4:c.170-75208G>A	NP_001785.2:n.170-75208G>A
NM_001794.5:c.170-75208G>A MANE Select	NP_001785.2:n.170-75208G>A
NM_001252339.3:c.-54+68366G>A	NP_001239268.1:n.-54+68366G>A