Canonical Allele Identifier: CA2373989252
Gene: CDH4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.61928306G= , CM000682.2:g.61928306G= GRCh38
NC_000020.10:g.60503364G= , CM000682.1:g.60503364G= GRCh37
NC_000020.9:g.59936759G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000614565.5:c.1888G= MANE Select ENSP00000484928.1:p.Ala630=
ENST00000543233.2:c.1666G= ENSP00000443301.1:p.Ala556=
ENST00000611855.4:c.1606G= ENSP00000480844.1:p.Ala536=
ENST00000614565.4:c.1888G= ENSP00000484928.1:p.Ala630=
NM_001252338.2:c.1777G= NP_001239267.1:p.Ala593=
NM_001252339.2:c.1666G= NP_001239268.1:p.Ala556=
NM_001794.4:c.1888G= NP_001785.2:p.Ala630=
NM_001794.5:c.1888G= MANE Select NP_001785.2:p.Ala630=
NM_001252339.3:c.1666G= NP_001239268.1:p.Ala556=