Canonical Allele Identifier: CA396462848

Gene: CDH1

Linked Data

• ClinVar Variation Id: 1010952
• ClinVar RCV Id: RCV001308675
• dbSNP Id: rs876659268
• MyVariant Identifiers: chr16:g.68849479C>A (hg19) ; chr16:g.68815576C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68815576C>A , CM000678.2:g.68815576C>A	GRCh38
NC_000016.9:g.68849479C>A , CM000678.1:g.68849479C>A	GRCh37
NC_000016.8:g.67406980C>A	NCBI36
NG_008021.1:g.83285C>A , LRG_301:g.83285C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000261769.10:c.1382C>A MANE Select	ENSP00000261769.4:p.Pro461His
ENST00000261769.9:c.1382C>A	ENSP00000261769.4:p.Pro461His
ENST00000422392.6:c.1199C>A	ENSP00000414946.2:p.Pro400His
ENST00000562836.5:n.1453C>A
ENST00000566510.5:c.*48C>A	ENSP00000458139.1:n.*48C>A
ENST00000566612.5:c.1382C>A	ENSP00000454782.1:p.Pro461His
ENST00000611625.4:c.1445C>A	ENSP00000481063.1:p.Pro482His
ENST00000612417.4:c.1382C>A	ENSP00000478360.1:p.Pro461His
ENST00000621016.4:c.1382C>A	ENSP00000480664.1:p.Pro461His
NM_004360.3:c.1382C>A , LRG_301t1:c.1382C>A	NP_004351.1:p.Pro461His
XM_011523488.1:c.647C>A	XP_011521790.1:p.Pro216His
XM_011523489.1:c.647C>A	XP_011521791.1:p.Pro216His
NM_001317184.1:c.1199C>A	NP_001304113.1:p.Pro400His
NM_001317185.1:c.-167C>A	NP_001304114.1:n.-167C>A
NM_001317186.1:c.-438C>A	NP_001304115.1:n.-438C>A
NM_004360.4:c.1382C>A	NP_004351.1:p.Pro461His
NM_004360.5:c.1382C>A MANE Select	NP_004351.1:p.Pro461His
NM_001317184.2:c.1199C>A	NP_001304113.1:p.Pro400His
NM_001317185.2:c.-167C>A	NP_001304114.1:n.-167C>A
NM_001317186.2:c.-438C>A	NP_001304115.1:n.-438C>A