Canonical Allele Identifier: CA1019080819
Gene: CDH4 HGNC NCBI

Linked Data

dbSNP Id: rs2084243440
gnomAD v3: 20-61278799-A-T
gnomAD v4: 20-61278799-A-T
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.61278799A>T , CM000682.2:g.61278799A>T GRCh38
NC_000020.10:g.59853855A>T , CM000682.1:g.59853855A>T GRCh37
NC_000020.9:g.59287250A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000614565.5:c.169+23862A>T MANE Select ENSP00000484928.1:n.169+23862A>T
ENST00000614565.4:c.169+23862A>T ENSP00000484928.1:n.169+23862A>T
NM_001794.4:c.169+23862A>T NP_001785.2:n.169+23862A>T
NM_001794.5:c.169+23862A>T MANE Select NP_001785.2:n.169+23862A>T
Search 100 bp 5'
Search 100 bp 3'