Canonical Allele Identifier: CA746323718
Gene: CDH4 HGNC NCBI

Linked Data

dbSNP Id: rs1307217880
gnomAD v3: 20-61928175-G-GT
gnomAD v4: 20-61928175-G-GT
MyVariant Identifiers: chr20:g.60503233_60503234insT (hg19) chr20:g.61928175_61928176insT (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.61928176dup , CM000682.2:g.61928176dup GRCh38
NC_000020.10:g.60503234dup , CM000682.1:g.60503234dup GRCh37
NC_000020.9:g.59936629dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000614565.5:c.1772-14dup MANE Select ENSP00000484928.1:n.1772-14dup
ENST00000543233.2:c.1550-14dup ENSP00000443301.1:n.1550-14dup
ENST00000611855.4:c.1490-14dup ENSP00000480844.1:n.1490-14dup
ENST00000614565.4:c.1772-14dup ENSP00000484928.1:n.1772-14dup
NM_001252338.2:c.1661-14dup NP_001239267.1:n.1661-14dup
NM_001252339.2:c.1550-14dup NP_001239268.1:n.1550-14dup
NM_001794.4:c.1772-14dup NP_001785.2:n.1772-14dup
NM_001794.5:c.1772-14dup MANE Select NP_001785.2:n.1772-14dup
NM_001252339.3:c.1550-14dup NP_001239268.1:n.1550-14dup
Search 100 bp 5'
Search 100 bp 3'