Canonical Allele Identifier: CA2373989134

Gene: CDH4

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.61928100_61928103delinsGGTT , CM000682.2:g.61928100_61928103delinsGGTT	GRCh38
NC_000020.10:g.60503158_60503161delinsGGTT , CM000682.1:g.60503158_60503161delinsGGTT	GRCh37
NC_000020.9:g.59936553_59936556delinsGGTT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000614565.5:c.1772-90_1772-87delinsGGTT MANE Select	ENSP00000484928.1:n.1772-90_1772-87delinsGGTT
ENST00000543233.2:c.1550-90_1550-87delinsGGTT	ENSP00000443301.1:n.1550-90_1550-87delinsGGTT
ENST00000611855.4:c.1490-90_1490-87delinsGGTT	ENSP00000480844.1:n.1490-90_1490-87delinsGGTT
ENST00000614565.4:c.1772-90_1772-87delinsGGTT	ENSP00000484928.1:n.1772-90_1772-87delinsGGTT
NM_001252338.2:c.1661-90_1661-87delinsGGTT	NP_001239267.1:n.1661-90_1661-87delinsGGTT
NM_001252339.2:c.1550-90_1550-87delinsGGTT	NP_001239268.1:n.1550-90_1550-87delinsGGTT
NM_001794.4:c.1772-90_1772-87delinsGGTT	NP_001785.2:n.1772-90_1772-87delinsGGTT
NM_001794.5:c.1772-90_1772-87delinsGGTT MANE Select	NP_001785.2:n.1772-90_1772-87delinsGGTT
NM_001252339.3:c.1550-90_1550-87delinsGGTT	NP_001239268.1:n.1550-90_1550-87delinsGGTT