Canonical Allele Identifier: CA2229916643

Gene: CDH1

Linked Data

• dbSNP Id: rs1962459558

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68738353_68738373dup , CM000678.2:g.68738353_68738373dup	GRCh38
NC_000016.9:g.68772256_68772276dup , CM000678.1:g.68772256_68772276dup	GRCh37
NC_000016.8:g.67329757_67329777dup	NCBI36
NG_008021.1:g.6062_6082dup , LRG_301:g.6062_6082dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261769.10:c.105_125dup MANE Select	ENSP00000261769.4:p.Pro42_Arg43insSerTyrThrPheThrValPro
ENST00000261769.9:c.105_125dup	ENSP00000261769.4:p.Pro42_Arg43insSerTyrThrPheThrValPro
ENST00000422392.6:c.105_125dup	ENSP00000414946.2:p.Pro42_Arg43insSerTyrThrPheThrValPro
ENST00000566510.5:c.105_125dup	ENSP00000458139.1:p.Pro42_Arg43insSerTyrThrPheThrValPro
ENST00000566612.5:c.105_125dup	ENSP00000454782.1:p.Pro42_Arg43insSerTyrThrPheThrValPro
ENST00000611625.4:c.105_125dup	ENSP00000481063.1:p.Pro42_Arg43insSerTyrThrPheThrValPro
ENST00000612417.4:c.105_125dup	ENSP00000478360.1:p.Pro42_Arg43insSerTyrThrPheThrValPro
ENST00000621016.4:c.105_125dup	ENSP00000480664.1:p.Pro42_Arg43insSerTyrThrPheThrValPro
NM_004360.3:c.105_125dup , LRG_301t1:c.105_125dup	NP_004351.1:p.Pro42_Arg43insSerTyrThrPheThrValPro
NM_001317184.1:c.105_125dup	NP_001304113.1:p.Pro42_Arg43insSerTyrThrPheThrValPro
NM_001317185.1:c.-1511_-1491dup	NP_001304114.1:n.-1511_-1491dup
NM_001317186.1:c.-1715_-1695dup	NP_001304115.1:n.-1715_-1695dup
NM_004360.4:c.105_125dup	NP_004351.1:p.Pro42_Arg43insSerTyrThrPheThrValPro
NM_004360.5:c.105_125dup MANE Select	NP_004351.1:p.Pro42_Arg43insSerTyrThrPheThrValPro
NM_001317184.2:c.105_125dup	NP_001304113.1:p.Pro42_Arg43insSerTyrThrPheThrValPro
NM_001317185.2:c.-1511_-1491dup	NP_001304114.1:n.-1511_-1491dup
NM_001317186.2:c.-1715_-1695dup	NP_001304115.1:n.-1715_-1695dup