Canonical Allele Identifier: CA3237904062
Gene: CDH4 HGNC NCBI

Genomic Alleles

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

Transcript Alleles

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