Canonical Allele Identifier: CA623140110

Gene: CDH1

Linked Data

• dbSNP Id: rs1216163892
• gnomAD v2: 16-68772244-CTTT-C
• gnomAD v3: 16-68738341-CTTT-C
• gnomAD v4: 16-68738341-CTTT-C
• MyVariant Identifiers: chr16:g.68772245_68772247del (hg19) ; chr16:g.68738342_68738344del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68738342_68738344del , CM000678.2:g.68738342_68738344del	GRCh38
NC_000016.9:g.68772245_68772247del , CM000678.1:g.68772245_68772247del	GRCh37
NC_000016.8:g.67329746_67329748del	NCBI36
NG_008021.1:g.6051_6053del , LRG_301:g.6051_6053del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261769.10:c.94_96del MANE Select	ENSP00000261769.4:p.Phe32del
ENST00000261769.9:c.94_96del	ENSP00000261769.4:p.Phe32del
ENST00000422392.6:c.94_96del	ENSP00000414946.2:p.Phe32del
ENST00000566510.5:c.94_96del	ENSP00000458139.1:p.Phe32del
ENST00000566612.5:c.94_96del	ENSP00000454782.1:p.Phe32del
ENST00000611625.4:c.94_96del	ENSP00000481063.1:p.Phe32del
ENST00000612417.4:c.94_96del	ENSP00000478360.1:p.Phe32del
ENST00000621016.4:c.94_96del	ENSP00000480664.1:p.Phe32del
NM_004360.3:c.94_96del , LRG_301t1:c.94_96del	NP_004351.1:p.Phe32del
NM_001317184.1:c.94_96del	NP_001304113.1:p.Phe32del
NM_001317185.1:c.-1522_-1520del	NP_001304114.1:n.-1522_-1520del
NM_001317186.1:c.-1726_-1724del	NP_001304115.1:n.-1726_-1724del
NM_004360.4:c.94_96del	NP_004351.1:p.Phe32del
NM_004360.5:c.94_96del MANE Select	NP_004351.1:p.Phe32del
NM_001317184.2:c.94_96del	NP_001304113.1:p.Phe32del
NM_001317185.2:c.-1522_-1520del	NP_001304114.1:n.-1522_-1520del
NM_001317186.2:c.-1726_-1724del	NP_001304115.1:n.-1726_-1724del