Canonical Allele Identifier: CA317137201

Gene: CDH4

Linked Data

• dbSNP Id: rs774811298
• gnomAD v4: 20-61928101-GTTGT-G
• MyVariant Identifiers: chr20:g.60503160_60503163del (hg19) ; chr20:g.61928102_61928105del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.61928106_61928109del , CM000682.2:g.61928106_61928109del	GRCh38
NC_000020.10:g.60503164_60503167del , CM000682.1:g.60503164_60503167del	GRCh37
NC_000020.9:g.59936559_59936562del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000614565.5:c.1772-84_1772-81del MANE Select	ENSP00000484928.1:n.1772-84_1772-81del
ENST00000543233.2:c.1550-84_1550-81del	ENSP00000443301.1:n.1550-84_1550-81del
ENST00000611855.4:c.1490-84_1490-81del	ENSP00000480844.1:n.1490-84_1490-81del
ENST00000614565.4:c.1772-84_1772-81del	ENSP00000484928.1:n.1772-84_1772-81del
NM_001252338.2:c.1661-84_1661-81del	NP_001239267.1:n.1661-84_1661-81del
NM_001252339.2:c.1550-84_1550-81del	NP_001239268.1:n.1550-84_1550-81del
NM_001794.4:c.1772-84_1772-81del	NP_001785.2:n.1772-84_1772-81del
NM_001794.5:c.1772-84_1772-81del MANE Select	NP_001785.2:n.1772-84_1772-81del
NM_001252339.3:c.1550-84_1550-81del	NP_001239268.1:n.1550-84_1550-81del