Canonical Allele Identifier: CA746323642
Gene: CDH4 HGNC NCBI

Linked Data

dbSNP Id: rs1304625256
gnomAD v3: 20-61928090-T-G
gnomAD v4: 20-61928090-T-G
MyVariant Identifiers: chr20:g.60503148T>G (hg19) chr20:g.61928090T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.61928090T>G , CM000682.2:g.61928090T>G GRCh38
NC_000020.10:g.60503148T>G , CM000682.1:g.60503148T>G GRCh37
NC_000020.9:g.59936543T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000614565.5:c.1772-100T>G MANE Select ENSP00000484928.1:n.1772-100T>G
ENST00000543233.2:c.1550-100T>G ENSP00000443301.1:n.1550-100T>G
ENST00000611855.4:c.1490-100T>G ENSP00000480844.1:n.1490-100T>G
ENST00000614565.4:c.1772-100T>G ENSP00000484928.1:n.1772-100T>G
NM_001252338.2:c.1661-100T>G NP_001239267.1:n.1661-100T>G
NM_001252339.2:c.1550-100T>G NP_001239268.1:n.1550-100T>G
NM_001794.4:c.1772-100T>G NP_001785.2:n.1772-100T>G
NM_001794.5:c.1772-100T>G MANE Select NP_001785.2:n.1772-100T>G
NM_001252339.3:c.1550-100T>G NP_001239268.1:n.1550-100T>G
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