Canonical Allele Identifier: CA317411494

Gene: CDH4

Linked Data

• dbSNP Id: rs544421786
• gnomAD v2: 20-60106894-C-T
• gnomAD v3: 20-61531838-C-T
• gnomAD v4: 20-61531838-C-T
• MyVariant Identifiers: chr20:g.60106894C>T (hg19) ; chr20:g.61531838C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.61531838C>T , CM000682.2:g.61531838C>T	GRCh38
NC_000020.10:g.60106894C>T , CM000682.1:g.60106894C>T	GRCh37
NC_000020.9:g.59540289C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000614565.5:c.170-211725C>T MANE Select	ENSP00000484928.1:n.170-211725C>T
ENST00000614565.4:c.170-211725C>T	ENSP00000484928.1:n.170-211725C>T
NM_001252338.2:c.58+32346C>T	NP_001239267.1:n.58+32346C>T
NM_001794.4:c.170-211725C>T	NP_001785.2:n.170-211725C>T
NM_001794.5:c.170-211725C>T MANE Select	NP_001785.2:n.170-211725C>T