Canonical Allele Identifier: CA409508662
Gene: CDH4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr20:g.60503278T>A (hg19) chr20:g.61928220T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.61928220T>A , CM000682.2:g.61928220T>A GRCh38
NC_000020.10:g.60503278T>A , CM000682.1:g.60503278T>A GRCh37
NC_000020.9:g.59936673T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000614565.5:c.1802T>A MANE Select ENSP00000484928.1:p.Leu601His
ENST00000543233.2:c.1580T>A ENSP00000443301.1:p.Leu527His
ENST00000611855.4:c.1520T>A ENSP00000480844.1:p.Leu507His
ENST00000614565.4:c.1802T>A ENSP00000484928.1:p.Leu601His
NM_001252338.2:c.1691T>A NP_001239267.1:p.Leu564His
NM_001252339.2:c.1580T>A NP_001239268.1:p.Leu527His
NM_001794.4:c.1802T>A NP_001785.2:p.Leu601His
NM_001794.5:c.1802T>A MANE Select NP_001785.2:p.Leu601His
NM_001252339.3:c.1580T>A NP_001239268.1:p.Leu527His
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