Canonical Allele Identifier: CA2373659737

Gene: CDH4

Linked Data

• dbSNP Id: rs2084242849

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.61278705T>C , CM000682.2:g.61278705T>C	GRCh38
NC_000020.10:g.59853761T>C , CM000682.1:g.59853761T>C	GRCh37
NC_000020.9:g.59287156T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000614565.5:c.169+23768T>C MANE Select	ENSP00000484928.1:n.169+23768T>C
ENST00000614565.4:c.169+23768T>C	ENSP00000484928.1:n.169+23768T>C
NM_001794.4:c.169+23768T>C	NP_001785.2:n.169+23768T>C
NM_001794.5:c.169+23768T>C MANE Select	NP_001785.2:n.169+23768T>C