Canonical Allele Identifier: CA746282134

Gene: CDH4

Linked Data

• dbSNP Id: rs1173917226
• MyVariant Identifiers: chr20:g.60106868_60106869del (hg19) ; chr20:g.61531812_61531813del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.61531812_61531813del , CM000682.2:g.61531812_61531813del	GRCh38
NC_000020.10:g.60106868_60106869del , CM000682.1:g.60106868_60106869del	GRCh37
NC_000020.9:g.59540263_59540264del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000614565.5:c.170-211751_170-211750del MANE Select	ENSP00000484928.1:n.170-211751_170-211750del
ENST00000614565.4:c.170-211751_170-211750del	ENSP00000484928.1:n.170-211751_170-211750del
NM_001252338.2:c.58+32320_58+32321del	NP_001239267.1:n.58+32320_58+32321del
NM_001794.4:c.170-211751_170-211750del	NP_001785.2:n.170-211751_170-211750del
NM_001794.5:c.170-211751_170-211750del MANE Select	NP_001785.2:n.170-211751_170-211750del