Canonical Allele Identifier: CA636608666

Gene: CDH4

Linked Data

• dbSNP Id: rs1387322056
• gnomAD v2: 20-60503204-A-AGTG
• gnomAD v4: 20-61928146-A-AGTG
• MyVariant Identifiers: chr20:g.60503204_60503205insGTG (hg19) ; chr20:g.61928146_61928147insGTG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.61928148_61928149insGGT , CM000682.2:g.61928148_61928149insGGT	GRCh38
NC_000020.10:g.60503206_60503207insGGT , CM000682.1:g.60503206_60503207insGGT	GRCh37
NC_000020.9:g.59936601_59936602insGGT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000614565.5:c.1772-42_1772-41insGGT MANE Select	ENSP00000484928.1:n.1772-42_1772-41insGGT
ENST00000543233.2:c.1550-42_1550-41insGGT	ENSP00000443301.1:n.1550-42_1550-41insGGT
ENST00000611855.4:c.1490-42_1490-41insGGT	ENSP00000480844.1:n.1490-42_1490-41insGGT
ENST00000614565.4:c.1772-42_1772-41insGGT	ENSP00000484928.1:n.1772-42_1772-41insGGT
NM_001252338.2:c.1661-42_1661-41insGGT	NP_001239267.1:n.1661-42_1661-41insGGT
NM_001252339.2:c.1550-42_1550-41insGGT	NP_001239268.1:n.1550-42_1550-41insGGT
NM_001794.4:c.1772-42_1772-41insGGT	NP_001785.2:n.1772-42_1772-41insGGT
NM_001794.5:c.1772-42_1772-41insGGT MANE Select	NP_001785.2:n.1772-42_1772-41insGGT
NM_001252339.3:c.1550-42_1550-41insGGT	NP_001239268.1:n.1550-42_1550-41insGGT