Canonical Allele Identifier: CA409508570
Gene: CDH4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr20:g.60503254C>A (hg19) chr20:g.61928196C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.61928196C>A , CM000682.2:g.61928196C>A GRCh38
NC_000020.10:g.60503254C>A , CM000682.1:g.60503254C>A GRCh37
NC_000020.9:g.59936649C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000614565.5:c.1778C>A MANE Select ENSP00000484928.1:p.Pro593His
ENST00000543233.2:c.1556C>A ENSP00000443301.1:p.Pro519His
ENST00000611855.4:c.1496C>A ENSP00000480844.1:p.Pro499His
ENST00000614565.4:c.1778C>A ENSP00000484928.1:p.Pro593His
NM_001252338.2:c.1667C>A NP_001239267.1:p.Pro556His
NM_001252339.2:c.1556C>A NP_001239268.1:p.Pro519His
NM_001794.4:c.1778C>A NP_001785.2:p.Pro593His
NM_001794.5:c.1778C>A MANE Select NP_001785.2:p.Pro593His
NM_001252339.3:c.1556C>A NP_001239268.1:p.Pro519His
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