Canonical Allele Identifier: CA511321939

Gene: CDH4

Linked Data

• dbSNP Id: rs767997015
• gnomAD v4: 20-61928200-G-C
• MyVariant Identifiers: chr20:g.60503258G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.61928200G>C , CM000682.2:g.61928200G>C	GRCh38
NC_000020.10:g.60503258G>C , CM000682.1:g.60503258G>C	GRCh37
NC_000020.9:g.59936653G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000614565.5:c.1782G>C MANE Select	ENSP00000484928.1:p.Pro594=
ENST00000543233.2:c.1560G>C	ENSP00000443301.1:p.Pro520=
ENST00000611855.4:c.1500G>C	ENSP00000480844.1:p.Pro500=
ENST00000614565.4:c.1782G>C	ENSP00000484928.1:p.Pro594=
NM_001252338.2:c.1671G>C	NP_001239267.1:p.Pro557=
NM_001252339.2:c.1560G>C	NP_001239268.1:p.Pro520=
NM_001794.4:c.1782G>C	NP_001785.2:p.Pro594=
NM_001794.5:c.1782G>C MANE Select	NP_001785.2:p.Pro594=
NM_001252339.3:c.1560G>C	NP_001239268.1:p.Pro520=