Canonical Allele Identifier: CA746323652

Gene: CDH4

Linked Data

• dbSNP Id: rs1463015941
• gnomAD v4: 20-61928100-GGTT-G
• MyVariant Identifiers: chr20:g.60503159_60503161del (hg19) ; chr20:g.61928101_61928103del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.61928104_61928106del , CM000682.2:g.61928104_61928106del	GRCh38
NC_000020.10:g.60503162_60503164del , CM000682.1:g.60503162_60503164del	GRCh37
NC_000020.9:g.59936557_59936559del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000614565.5:c.1772-86_1772-84del MANE Select	ENSP00000484928.1:n.1772-86_1772-84del
ENST00000543233.2:c.1550-86_1550-84del	ENSP00000443301.1:n.1550-86_1550-84del
ENST00000611855.4:c.1490-86_1490-84del	ENSP00000480844.1:n.1490-86_1490-84del
ENST00000614565.4:c.1772-86_1772-84del	ENSP00000484928.1:n.1772-86_1772-84del
NM_001252338.2:c.1661-86_1661-84del	NP_001239267.1:n.1661-86_1661-84del
NM_001252339.2:c.1550-86_1550-84del	NP_001239268.1:n.1550-86_1550-84del
NM_001794.4:c.1772-86_1772-84del	NP_001785.2:n.1772-86_1772-84del
NM_001794.5:c.1772-86_1772-84del MANE Select	NP_001785.2:n.1772-86_1772-84del
NM_001252339.3:c.1550-86_1550-84del	NP_001239268.1:n.1550-86_1550-84del