Canonical Allele Identifier: CA746323639

Gene: CDH4

Linked Data

• dbSNP Id: rs1228136078
• gnomAD v3: 20-61928082-CCT-C
• gnomAD v4: 20-61928082-CCT-C
• MyVariant Identifiers: chr20:g.60503141_60503142del (hg19) ; chr20:g.61928083_61928084del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.61928083_61928084del , CM000682.2:g.61928083_61928084del	GRCh38
NC_000020.10:g.60503141_60503142del , CM000682.1:g.60503141_60503142del	GRCh37
NC_000020.9:g.59936536_59936537del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000614565.5:c.1772-107_1772-106del MANE Select	ENSP00000484928.1:n.1772-107_1772-106del
ENST00000543233.2:c.1550-107_1550-106del	ENSP00000443301.1:n.1550-107_1550-106del
ENST00000611855.4:c.1490-107_1490-106del	ENSP00000480844.1:n.1490-107_1490-106del
ENST00000614565.4:c.1772-107_1772-106del	ENSP00000484928.1:n.1772-107_1772-106del
NM_001252338.2:c.1661-107_1661-106del	NP_001239267.1:n.1661-107_1661-106del
NM_001252339.2:c.1550-107_1550-106del	NP_001239268.1:n.1550-107_1550-106del
NM_001794.4:c.1772-107_1772-106del	NP_001785.2:n.1772-107_1772-106del
NM_001794.5:c.1772-107_1772-106del MANE Select	NP_001785.2:n.1772-107_1772-106del
NM_001252339.3:c.1550-107_1550-106del	NP_001239268.1:n.1550-107_1550-106del