Canonical Allele Identifier: CA299004

Gene: CDH1

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68823488G>A , CM000678.2:g.68823488G>A	GRCh38
NC_000016.9:g.68857391G>A , CM000678.1:g.68857391G>A	GRCh37
NC_000016.8:g.67414892G>A	NCBI36
NG_008021.1:g.91197G>A , LRG_301:g.91197G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261769.10:c.2026G>A MANE Select	ENSP00000261769.4:p.Asp676Asn
ENST00000261769.9:c.2026G>A	ENSP00000261769.4:p.Asp676Asn
ENST00000422392.6:c.1843G>A	ENSP00000414946.2:p.Asp615Asn
ENST00000562118.1:n.244G>A
ENST00000562836.5:n.2097G>A
ENST00000566510.5:c.*692G>A	ENSP00000458139.1:n.*692G>A
ENST00000566612.5:c.*266G>A	ENSP00000454782.1:n.*266G>A
ENST00000611625.4:c.2089G>A	ENSP00000481063.1:p.Asp697Asn
ENST00000612417.4:c.1830+1369G>A	ENSP00000478360.1:n.1830+1369G>A
ENST00000621016.4:c.1865+1334G>A	ENSP00000480664.1:n.1865+1334G>A
NM_004360.3:c.2026G>A , LRG_301t1:c.2026G>A	NP_004351.1:p.Asp676Asn
XM_011523488.1:c.1291G>A	XP_011521790.1:p.Asp431Asn
XM_011523489.1:c.1291G>A	XP_011521791.1:p.Asp431Asn
NM_001317184.1:c.1843G>A	NP_001304113.1:p.Asp615Asn
NM_001317185.1:c.478G>A	NP_001304114.1:p.Asp160Asn
NM_001317186.1:c.61G>A	NP_001304115.1:p.Asp21Asn
NM_004360.4:c.2026G>A	NP_004351.1:p.Asp676Asn
NM_004360.5:c.2026G>A MANE Select	NP_004351.1:p.Asp676Asn
NM_001317184.2:c.1843G>A	NP_001304113.1:p.Asp615Asn
NM_001317185.2:c.478G>A	NP_001304114.1:p.Asp160Asn
NM_001317186.2:c.61G>A	NP_001304115.1:p.Asp21Asn