Canonical Allele Identifier: CA1019134402

Gene: CDH4

Linked Data

• dbSNP Id: rs2055064623
• gnomAD v3: 20-61928109-T-TGTGC
• gnomAD v4: 20-61928109-T-TGTGC

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.61928113_61928116dup , CM000682.2:g.61928113_61928116dup	GRCh38
NC_000020.10:g.60503171_60503174dup , CM000682.1:g.60503171_60503174dup	GRCh37
NC_000020.9:g.59936566_59936569dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000614565.5:c.1772-77_1772-74dup MANE Select	ENSP00000484928.1:n.1772-77_1772-74dup
ENST00000543233.2:c.1550-77_1550-74dup	ENSP00000443301.1:n.1550-77_1550-74dup
ENST00000611855.4:c.1490-77_1490-74dup	ENSP00000480844.1:n.1490-77_1490-74dup
ENST00000614565.4:c.1772-77_1772-74dup	ENSP00000484928.1:n.1772-77_1772-74dup
NM_001252338.2:c.1661-77_1661-74dup	NP_001239267.1:n.1661-77_1661-74dup
NM_001252339.2:c.1550-77_1550-74dup	NP_001239268.1:n.1550-77_1550-74dup
NM_001794.4:c.1772-77_1772-74dup	NP_001785.2:n.1772-77_1772-74dup
NM_001794.5:c.1772-77_1772-74dup MANE Select	NP_001785.2:n.1772-77_1772-74dup
NM_001252339.3:c.1550-77_1550-74dup	NP_001239268.1:n.1550-77_1550-74dup