Canonical Allele Identifier: CA511322229

Gene: CDH4

Linked Data

• gnomAD v4: 20-61928323-G-T
• MyVariant Identifiers: chr20:g.60503381G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.61928323G>T , CM000682.2:g.61928323G>T	GRCh38
NC_000020.10:g.60503381G>T , CM000682.1:g.60503381G>T	GRCh37
NC_000020.9:g.59936776G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000614565.5:c.1905G>T MANE Select	ENSP00000484928.1:p.Ala635=
ENST00000543233.2:c.1683G>T	ENSP00000443301.1:p.Ala561=
ENST00000611855.4:c.1623G>T	ENSP00000480844.1:p.Ala541=
ENST00000614565.4:c.1905G>T	ENSP00000484928.1:p.Ala635=
NM_001252338.2:c.1794G>T	NP_001239267.1:p.Ala598=
NM_001252339.2:c.1683G>T	NP_001239268.1:p.Ala561=
NM_001794.4:c.1905G>T	NP_001785.2:p.Ala635=
NM_001794.5:c.1905G>T MANE Select	NP_001785.2:p.Ala635=
NM_001252339.3:c.1683G>T	NP_001239268.1:p.Ala561=