Canonical Allele Identifier: CA2373659811
Gene: CDH4 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.61278858A= , CM000682.2:g.61278858A= GRCh38
NC_000020.10:g.59853914A= , CM000682.1:g.59853914A= GRCh37
NC_000020.9:g.59287309A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000614565.5:c.169+23921A= MANE Select ENSP00000484928.1:n.169+23921A=
ENST00000614565.4:c.169+23921A= ENSP00000484928.1:n.169+23921A=
NM_001794.4:c.169+23921A= NP_001785.2:n.169+23921A=
NM_001794.5:c.169+23921A= MANE Select NP_001785.2:n.169+23921A=
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