Canonical Allele Identifier: CA511322100
Gene: CDH4 HGNC NCBI

Linked Data

gnomAD v4: 20-61928230-T-C
MyVariant Identifiers: chr20:g.60503288T>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.61928230T>C , CM000682.2:g.61928230T>C GRCh38
NC_000020.10:g.60503288T>C , CM000682.1:g.60503288T>C GRCh37
NC_000020.9:g.59936683T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000614565.5:c.1812T>C MANE Select ENSP00000484928.1:p.Tyr604=
ENST00000543233.2:c.1590T>C ENSP00000443301.1:p.Tyr530=
ENST00000611855.4:c.1530T>C ENSP00000480844.1:p.Tyr510=
ENST00000614565.4:c.1812T>C ENSP00000484928.1:p.Tyr604=
NM_001252338.2:c.1701T>C NP_001239267.1:p.Tyr567=
NM_001252339.2:c.1590T>C NP_001239268.1:p.Tyr530=
NM_001794.4:c.1812T>C NP_001785.2:p.Tyr604=
NM_001794.5:c.1812T>C MANE Select NP_001785.2:p.Tyr604=
NM_001252339.3:c.1590T>C NP_001239268.1:p.Tyr530=
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