Canonical Allele Identifier: CA409508565
Gene: CDH4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr20:g.60503253C>A (hg19) chr20:g.61928195C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.61928195C>A , CM000682.2:g.61928195C>A GRCh38
NC_000020.10:g.60503253C>A , CM000682.1:g.60503253C>A GRCh37
NC_000020.9:g.59936648C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000614565.5:c.1777C>A MANE Select ENSP00000484928.1:p.Pro593Thr
ENST00000543233.2:c.1555C>A ENSP00000443301.1:p.Pro519Thr
ENST00000611855.4:c.1495C>A ENSP00000480844.1:p.Pro499Thr
ENST00000614565.4:c.1777C>A ENSP00000484928.1:p.Pro593Thr
NM_001252338.2:c.1666C>A NP_001239267.1:p.Pro556Thr
NM_001252339.2:c.1555C>A NP_001239268.1:p.Pro519Thr
NM_001794.4:c.1777C>A NP_001785.2:p.Pro593Thr
NM_001794.5:c.1777C>A MANE Select NP_001785.2:p.Pro593Thr
NM_001252339.3:c.1555C>A NP_001239268.1:p.Pro519Thr
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