Canonical Allele Identifier: CA2229957792

Gene: CDH1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68801783A= , CM000678.2:g.68801783A=	GRCh38
NC_000016.9:g.68835686A= , CM000678.1:g.68835686A=	GRCh37
NC_000016.8:g.67393187A=	NCBI36
NG_008021.1:g.69492A= , LRG_301:g.69492A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000261769.10:c.277A= MANE Select	ENSP00000261769.4:p.Asn93=
ENST00000261769.9:c.277A=	ENSP00000261769.4:p.Asn93=
ENST00000422392.6:c.277A=	ENSP00000414946.2:p.Asn93=
ENST00000561751.1:c.44A=
ENST00000562836.5:n.348A=
ENST00000564676.5:n.559A=
ENST00000564745.1:n.272A=
ENST00000566510.5:c.277A=	ENSP00000458139.1:p.Asn93=
ENST00000566612.5:c.277A=	ENSP00000454782.1:p.Asn93=
ENST00000611625.4:c.277A=	ENSP00000481063.1:p.Asn93=
ENST00000612417.4:c.277A=	ENSP00000478360.1:p.Asn93=
ENST00000621016.4:c.277A=	ENSP00000480664.1:p.Asn93=
NM_004360.3:c.277A= , LRG_301t1:c.277A=	NP_004351.1:p.Asn93=
XM_011523488.1:c.-459A=	XP_011521790.1:n.-459A=
XM_011523489.1:c.-459A=	XP_011521791.1:n.-459A=
NM_001317184.1:c.277A=	NP_001304113.1:p.Asn93=
NM_001317185.1:c.-1339A=	NP_001304114.1:n.-1339A=
NM_001317186.1:c.-1543A=	NP_001304115.1:n.-1543A=
NM_004360.4:c.277A=	NP_004351.1:p.Asn93=
NM_004360.5:c.277A= MANE Select	NP_004351.1:p.Asn93=
NM_001317184.2:c.277A=	NP_001304113.1:p.Asn93=
NM_001317185.2:c.-1339A=	NP_001304114.1:n.-1339A=
NM_001317186.2:c.-1543A=	NP_001304115.1:n.-1543A=