Canonical Allele Identifier: CA2373989293
Gene: CDH4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.61928382C= , CM000682.2:g.61928382C= GRCh38
NC_000020.10:g.60503440C= , CM000682.1:g.60503440C= GRCh37
NC_000020.9:g.59936835C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000614565.5:c.1964C= MANE Select ENSP00000484928.1:p.Pro655=
ENST00000543233.2:c.1742C= ENSP00000443301.1:p.Pro581=
ENST00000611855.4:c.1682C= ENSP00000480844.1:p.Pro561=
ENST00000614565.4:c.1964C= ENSP00000484928.1:p.Pro655=
NM_001252338.2:c.1853C= NP_001239267.1:p.Pro618=
NM_001252339.2:c.1742C= NP_001239268.1:p.Pro581=
NM_001794.4:c.1964C= NP_001785.2:p.Pro655=
NM_001794.5:c.1964C= MANE Select NP_001785.2:p.Pro655=
NM_001252339.3:c.1742C= NP_001239268.1:p.Pro581=