Canonical Allele Identifier: CA2373989258
Gene: CDH4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.61928316T= , CM000682.2:g.61928316T= GRCh38
NC_000020.10:g.60503374T= , CM000682.1:g.60503374T= GRCh37
NC_000020.9:g.59936769T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000614565.5:c.1898T= MANE Select ENSP00000484928.1:p.Ile633=
ENST00000543233.2:c.1676T= ENSP00000443301.1:p.Ile559=
ENST00000611855.4:c.1616T= ENSP00000480844.1:p.Ile539=
ENST00000614565.4:c.1898T= ENSP00000484928.1:p.Ile633=
NM_001252338.2:c.1787T= NP_001239267.1:p.Ile596=
NM_001252339.2:c.1676T= NP_001239268.1:p.Ile559=
NM_001794.4:c.1898T= NP_001785.2:p.Ile633=
NM_001794.5:c.1898T= MANE Select NP_001785.2:p.Ile633=
NM_001252339.3:c.1676T= NP_001239268.1:p.Ile559=