Canonical Allele Identifier: CA2582342541

Gene: CDH1

Linked Data

• ClinVar Variation Id: 2583748
• ClinVar RCV Id: RCV003334670

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68737457dup , CM000678.2:g.68737457dup	GRCh38
NC_000016.9:g.68771360dup , CM000678.1:g.68771360dup	GRCh37
NC_000016.8:g.67328861dup	NCBI36
NG_008021.1:g.5166dup , LRG_301:g.5166dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261769.10:c.42dup MANE Select	ENSP00000261769.4:p.Leu15AlafsTer19
ENST00000261769.9:c.42dup	ENSP00000261769.4:p.Leu15AlafsTer19
ENST00000422392.6:c.42dup	ENSP00000414946.2:p.Leu15AlafsTer19
ENST00000566510.5:c.42dup	ENSP00000458139.1:p.Leu15AlafsTer19
ENST00000566612.5:c.42dup	ENSP00000454782.1:p.Leu15AlafsTer19
ENST00000611625.4:c.42dup	ENSP00000481063.1:p.Leu15AlafsTer19
ENST00000612417.4:c.42dup	ENSP00000478360.1:p.Leu15AlafsTer19
ENST00000621016.4:c.42dup	ENSP00000480664.1:p.Leu15AlafsTer19
NM_004360.3:c.42dup , LRG_301t1:c.42dup	NP_004351.1:p.Leu15AlafsTer19
NM_001317184.1:c.42dup	NP_001304113.1:p.Leu15AlafsTer19
NM_001317185.1:c.-1574dup	NP_001304114.1:n.-1574dup
NM_001317186.1:c.-1778dup	NP_001304115.1:n.-1778dup
NM_004360.4:c.42dup	NP_004351.1:p.Leu15AlafsTer19
NM_004360.5:c.42dup MANE Select	NP_004351.1:p.Leu15AlafsTer19
NM_001317184.2:c.42dup	NP_001304113.1:p.Leu15AlafsTer19
NM_001317185.2:c.-1574dup	NP_001304114.1:n.-1574dup
NM_001317186.2:c.-1778dup	NP_001304115.1:n.-1778dup