Canonical Allele Identifier: CA317134274
Gene: CDH4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.61668355G>T , CM000682.2:g.61668355G>T GRCh38
NC_000020.10:g.60243411G>T , CM000682.1:g.60243411G>T GRCh37
NC_000020.9:g.59676806G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000614565.5:c.170-75208G>T MANE Select ENSP00000484928.1:n.170-75208G>T
ENST00000543233.2:c.-54+68366G>T ENSP00000443301.1:n.-54+68366G>T
ENST00000611855.4:c.50-75208G>T ENSP00000480844.1:n.50-75208G>T
ENST00000614565.4:c.170-75208G>T ENSP00000484928.1:n.170-75208G>T
NM_001252338.2:c.59-75208G>T NP_001239267.1:n.59-75208G>T
NM_001252339.2:c.-54+68366G>T NP_001239268.1:n.-54+68366G>T
NM_001794.4:c.170-75208G>T NP_001785.2:n.170-75208G>T
NM_001794.5:c.170-75208G>T MANE Select NP_001785.2:n.170-75208G>T
NM_001252339.3:c.-54+68366G>T NP_001239268.1:n.-54+68366G>T