Canonical Allele Identifier: CA2373863014

Gene: CDH4

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.61683795G= , CM000682.2:g.61683795G=	GRCh38
NC_000020.10:g.60258851G= , CM000682.1:g.60258851G=	GRCh37
NC_000020.9:g.59692246G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001794.5:c.170-59768G= MANE Select	NP_001785.2:n.170-59768G=
ENST00000614565.5:c.170-59768G= MANE Select	ENSP00000484928.1:n.170-59768G=
NM_001252338.2:c.59-59768G=	NP_001239267.1:n.59-59768G=
NM_001252339.2:c.-53-59768G=	NP_001239268.1:n.-53-59768G=
NM_001252339.3:c.-53-59768G=	NP_001239268.1:n.-53-59768G=
NM_001794.4:c.170-59768G=	NP_001785.2:n.170-59768G=
ENST00000543233.2:c.-53-59768G=	ENSP00000443301.1:n.-53-59768G=
ENST00000611855.4:c.50-59768G=	ENSP00000480844.1:n.50-59768G=
ENST00000614565.4:c.170-59768G=	ENSP00000484928.1:n.170-59768G=