Canonical Allele Identifier: CA317411398
Gene: CDH4 HGNC NCBI

Linked Data

dbSNP Id: rs8123637
MyVariant Identifiers: chr20:g.60106758G>A (hg19) chr20:g.61531702G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.61531702G>A , CM000682.2:g.61531702G>A GRCh38
NC_000020.10:g.60106758G>A , CM000682.1:g.60106758G>A GRCh37
NC_000020.9:g.59540153G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000614565.5:c.170-211861G>A MANE Select ENSP00000484928.1:n.170-211861G>A
ENST00000614565.4:c.170-211861G>A ENSP00000484928.1:n.170-211861G>A
NM_001252338.2:c.58+32210G>A NP_001239267.1:n.58+32210G>A
NM_001794.4:c.170-211861G>A NP_001785.2:n.170-211861G>A
NM_001794.5:c.170-211861G>A MANE Select NP_001785.2:n.170-211861G>A
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