Canonical Allele Identifier: CA891842210

Gene: CDH1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68810323_68810334del , CM000678.2:g.68810323_68810334del	GRCh38
NC_000016.9:g.68844226_68844237del , CM000678.1:g.68844226_68844237del	GRCh37
NC_000016.8:g.67401727_67401738del	NCBI36
NG_008021.1:g.78032_78043del , LRG_301:g.78032_78043del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261769.10:c.814_825del MANE Select	ENSP00000261769.4:p.Met272_Ala275del
ENST00000261769.9:c.814_825del	ENSP00000261769.4:p.Met272_Ala275del
ENST00000422392.6:c.814_825del	ENSP00000414946.2:p.Met272_Ala275del
ENST00000561751.1:c.455-1361_455-1350del
ENST00000562836.5:n.885_896del
ENST00000566510.5:c.658_669del	ENSP00000458139.1:p.Met220_Ala223del
ENST00000566612.5:c.814_825del	ENSP00000454782.1:p.Met272_Ala275del
ENST00000611625.4:c.814_825del	ENSP00000481063.1:p.Met272_Ala275del
ENST00000612417.4:c.814_825del	ENSP00000478360.1:p.Met272_Ala275del
ENST00000621016.4:c.814_825del	ENSP00000480664.1:p.Met272_Ala275del
NM_004360.3:c.814_825del , LRG_301t1:c.814_825del	NP_004351.1:p.Met272_Ala275del
XM_011523488.1:c.79_90del	XP_011521790.1:p.Met27_Ala30del
XM_011523489.1:c.79_90del	XP_011521791.1:p.Met27_Ala30del
NM_001317184.1:c.814_825del	NP_001304113.1:p.Met272_Ala275del
NM_001317185.1:c.-802_-791del	NP_001304114.1:n.-802_-791del
NM_001317186.1:c.-1006_-995del	NP_001304115.1:n.-1006_-995del
NM_004360.4:c.814_825del	NP_004351.1:p.Met272_Ala275del
NM_004360.5:c.814_825del MANE Select	NP_004351.1:p.Met272_Ala275del
NM_001317184.2:c.814_825del	NP_001304113.1:p.Met272_Ala275del
NM_001317185.2:c.-802_-791del	NP_001304114.1:n.-802_-791del
NM_001317186.2:c.-1006_-995del	NP_001304115.1:n.-1006_-995del