Canonical Allele Identifier: CA409509149

Gene: CDH4

Linked Data

• MyVariant Identifiers: chr20:g.60503386A>C (hg19) ; chr20:g.61928328A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.61928328A>C , CM000682.2:g.61928328A>C	GRCh38
NC_000020.10:g.60503386A>C , CM000682.1:g.60503386A>C	GRCh37
NC_000020.9:g.59936781A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000614565.5:c.1910A>C MANE Select	ENSP00000484928.1:p.Asp637Ala
ENST00000543233.2:c.1688A>C	ENSP00000443301.1:p.Asp563Ala
ENST00000611855.4:c.1628A>C	ENSP00000480844.1:p.Asp543Ala
ENST00000614565.4:c.1910A>C	ENSP00000484928.1:p.Asp637Ala
NM_001252338.2:c.1799A>C	NP_001239267.1:p.Asp600Ala
NM_001252339.2:c.1688A>C	NP_001239268.1:p.Asp563Ala
NM_001794.4:c.1910A>C	NP_001785.2:p.Asp637Ala
NM_001794.5:c.1910A>C MANE Select	NP_001785.2:p.Asp637Ala
NM_001252339.3:c.1688A>C	NP_001239268.1:p.Asp563Ala