Canonical Allele Identifier: CA2736964107
Gene: CDH4 HGNC NCBI

Linked Data

dbSNP Id: rs2122990720

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.61928180T>G , CM000682.2:g.61928180T>G GRCh38
NC_000020.10:g.60503238T>G , CM000682.1:g.60503238T>G GRCh37
NC_000020.9:g.59936633T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000614565.5:c.1772-10T>G MANE Select ENSP00000484928.1:n.1772-10T>G
ENST00000543233.2:c.1550-10T>G ENSP00000443301.1:n.1550-10T>G
ENST00000611855.4:c.1490-10T>G ENSP00000480844.1:n.1490-10T>G
ENST00000614565.4:c.1772-10T>G ENSP00000484928.1:n.1772-10T>G
NM_001252338.2:c.1661-10T>G NP_001239267.1:n.1661-10T>G
NM_001252339.2:c.1550-10T>G NP_001239268.1:n.1550-10T>G
NM_001794.4:c.1772-10T>G NP_001785.2:n.1772-10T>G
NM_001794.5:c.1772-10T>G MANE Select NP_001785.2:n.1772-10T>G
NM_001252339.3:c.1550-10T>G NP_001239268.1:n.1550-10T>G