Canonical Allele Identifier: CA2373989135

Gene: CDH4

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.61928101_61928105delinsGTTGT , CM000682.2:g.61928101_61928105delinsGTTGT	GRCh38
NC_000020.10:g.60503159_60503163delinsGTTGT , CM000682.1:g.60503159_60503163delinsGTTGT	GRCh37
NC_000020.9:g.59936554_59936558delinsGTTGT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000614565.5:c.1772-89_1772-85delinsGTTGT MANE Select	ENSP00000484928.1:n.1772-89_1772-85delinsGTTGT
ENST00000543233.2:c.1550-89_1550-85delinsGTTGT	ENSP00000443301.1:n.1550-89_1550-85delinsGTTGT
ENST00000611855.4:c.1490-89_1490-85delinsGTTGT	ENSP00000480844.1:n.1490-89_1490-85delinsGTTGT
ENST00000614565.4:c.1772-89_1772-85delinsGTTGT	ENSP00000484928.1:n.1772-89_1772-85delinsGTTGT
NM_001252338.2:c.1661-89_1661-85delinsGTTGT	NP_001239267.1:n.1661-89_1661-85delinsGTTGT
NM_001252339.2:c.1550-89_1550-85delinsGTTGT	NP_001239268.1:n.1550-89_1550-85delinsGTTGT
NM_001794.4:c.1772-89_1772-85delinsGTTGT	NP_001785.2:n.1772-89_1772-85delinsGTTGT
NM_001794.5:c.1772-89_1772-85delinsGTTGT MANE Select	NP_001785.2:n.1772-89_1772-85delinsGTTGT
NM_001252339.3:c.1550-89_1550-85delinsGTTGT	NP_001239268.1:n.1550-89_1550-85delinsGTTGT