Canonical Allele Identifier: CA9934918
Gene: CDH4 HGNC NCBI

Linked Data

dbSNP Id: rs754772940

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.61928366G>A , CM000682.2:g.61928366G>A GRCh38
NC_000020.10:g.60503424G>A , CM000682.1:g.60503424G>A GRCh37
NC_000020.9:g.59936819G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000614565.5:c.1948G>A MANE Select ENSP00000484928.1:p.Glu650Lys
ENST00000543233.2:c.1726G>A ENSP00000443301.1:p.Glu576Lys
ENST00000611855.4:c.1666G>A ENSP00000480844.1:p.Glu556Lys
ENST00000614565.4:c.1948G>A ENSP00000484928.1:p.Glu650Lys
NM_001252338.2:c.1837G>A NP_001239267.1:p.Glu613Lys
NM_001252339.2:c.1726G>A NP_001239268.1:p.Glu576Lys
NM_001794.4:c.1948G>A NP_001785.2:p.Glu650Lys
NM_001794.5:c.1948G>A MANE Select NP_001785.2:p.Glu650Lys
NM_001252339.3:c.1726G>A NP_001239268.1:p.Glu576Lys