Canonical Allele Identifier: CA2373989130
Gene: CDH4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.61928089A= , CM000682.2:g.61928089A= GRCh38
NC_000020.10:g.60503147A= , CM000682.1:g.60503147A= GRCh37
NC_000020.9:g.59936542A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000614565.5:c.1772-101A= MANE Select ENSP00000484928.1:n.1772-101A=
ENST00000543233.2:c.1550-101A= ENSP00000443301.1:n.1550-101A=
ENST00000611855.4:c.1490-101A= ENSP00000480844.1:n.1490-101A=
ENST00000614565.4:c.1772-101A= ENSP00000484928.1:n.1772-101A=
NM_001252338.2:c.1661-101A= NP_001239267.1:n.1661-101A=
NM_001252339.2:c.1550-101A= NP_001239268.1:n.1550-101A=
NM_001794.4:c.1772-101A= NP_001785.2:n.1772-101A=
NM_001794.5:c.1772-101A= MANE Select NP_001785.2:n.1772-101A=
NM_001252339.3:c.1550-101A= NP_001239268.1:n.1550-101A=