Canonical Allele Identifier: CA409508762
Gene: CDH4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr20:g.60503299T>C (hg19) chr20:g.61928241T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.61928241T>C , CM000682.2:g.61928241T>C GRCh38
NC_000020.10:g.60503299T>C , CM000682.1:g.60503299T>C GRCh37
NC_000020.9:g.59936694T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000614565.5:c.1823T>C MANE Select ENSP00000484928.1:p.Ile608Thr
ENST00000543233.2:c.1601T>C ENSP00000443301.1:p.Ile534Thr
ENST00000611855.4:c.1541T>C ENSP00000480844.1:p.Ile514Thr
ENST00000614565.4:c.1823T>C ENSP00000484928.1:p.Ile608Thr
NM_001252338.2:c.1712T>C NP_001239267.1:p.Ile571Thr
NM_001252339.2:c.1601T>C NP_001239268.1:p.Ile534Thr
NM_001794.4:c.1823T>C NP_001785.2:p.Ile608Thr
NM_001794.5:c.1823T>C MANE Select NP_001785.2:p.Ile608Thr
NM_001252339.3:c.1601T>C NP_001239268.1:p.Ile534Thr
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