Canonical Allele Identifier: CA746282064
Gene: CDH4 HGNC NCBI

Linked Data

dbSNP Id: rs1280542991
MyVariant Identifiers: chr20:g.60106757A>G (hg19) chr20:g.61531701A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.61531701A>G , CM000682.2:g.61531701A>G GRCh38
NC_000020.10:g.60106757A>G , CM000682.1:g.60106757A>G GRCh37
NC_000020.9:g.59540152A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000614565.5:c.170-211862A>G MANE Select ENSP00000484928.1:n.170-211862A>G
ENST00000614565.4:c.170-211862A>G ENSP00000484928.1:n.170-211862A>G
NM_001252338.2:c.58+32209A>G NP_001239267.1:n.58+32209A>G
NM_001794.4:c.170-211862A>G NP_001785.2:n.170-211862A>G
NM_001794.5:c.170-211862A>G MANE Select NP_001785.2:n.170-211862A>G
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