Canonical Allele Identifier: CA2697554037

Gene: CDH1

Linked Data

• ClinVar Variation Id: 2719428
• ClinVar RCV Id: RCV003513253
• dbSNP Id: rs1432324307

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68808686T>A , CM000678.2:g.68808686T>A	GRCh38
NC_000016.9:g.68842589T>A , CM000678.1:g.68842589T>A	GRCh37
NC_000016.8:g.67400090T>A	NCBI36
NG_008021.1:g.76395T>A , LRG_301:g.76395T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000261769.10:c.532-7T>A MANE Select	ENSP00000261769.4:n.532-7T>A
ENST00000261769.9:c.532-7T>A	ENSP00000261769.4:n.532-7T>A
ENST00000422392.6:c.532-7T>A	ENSP00000414946.2:n.532-7T>A
ENST00000561751.1:c.299-7T>A
ENST00000562836.5:n.603-7T>A
ENST00000564676.5:n.814-7T>A
ENST00000564745.1:n.527-7T>A
ENST00000566510.5:c.531+119T>A	ENSP00000458139.1:n.531+119T>A
ENST00000566612.5:c.532-7T>A	ENSP00000454782.1:n.532-7T>A
ENST00000567320.1:n.42-7T>A
ENST00000611625.4:c.532-7T>A	ENSP00000481063.1:n.532-7T>A
ENST00000612417.4:c.532-7T>A	ENSP00000478360.1:n.532-7T>A
ENST00000621016.4:c.532-7T>A	ENSP00000480664.1:n.532-7T>A
NM_004360.3:c.532-7T>A , LRG_301t1:c.532-7T>A	NP_004351.1:n.532-7T>A
XM_011523488.1:c.-204-7T>A	XP_011521790.1:n.-204-7T>A
XM_011523489.1:c.-204-7T>A	XP_011521791.1:n.-204-7T>A
NM_001317184.1:c.532-7T>A	NP_001304113.1:n.532-7T>A
NM_001317185.1:c.-1084-7T>A	NP_001304114.1:n.-1084-7T>A
NM_001317186.1:c.-1288-7T>A	NP_001304115.1:n.-1288-7T>A
NM_004360.4:c.532-7T>A	NP_004351.1:n.532-7T>A
NM_004360.5:c.532-7T>A MANE Select	NP_004351.1:n.532-7T>A
NM_001317184.2:c.532-7T>A	NP_001304113.1:n.532-7T>A
NM_001317185.2:c.-1084-7T>A	NP_001304114.1:n.-1084-7T>A
NM_001317186.2:c.-1288-7T>A	NP_001304115.1:n.-1288-7T>A