Canonical Allele Identifier: CA396451616

Gene: CDH1

Linked Data

• ClinVar Variation Id: 479528
• ClinVar RCV Id: RCV003327424
• dbSNP Id: rs1221633501
• MyVariant Identifiers: chr16:g.68772207C>G (hg19) ; chr16:g.68738304C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68738304C>G , CM000678.2:g.68738304C>G	GRCh38
NC_000016.9:g.68772207C>G , CM000678.1:g.68772207C>G	GRCh37
NC_000016.8:g.67329708C>G	NCBI36
NG_008021.1:g.6013C>G , LRG_301:g.6013C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000261769.10:c.56C>G MANE Select	ENSP00000261769.4:p.Ser19Cys
ENST00000261769.9:c.56C>G	ENSP00000261769.4:p.Ser19Cys
ENST00000422392.6:c.56C>G	ENSP00000414946.2:p.Ser19Cys
ENST00000566510.5:c.56C>G	ENSP00000458139.1:p.Ser19Cys
ENST00000566612.5:c.56C>G	ENSP00000454782.1:p.Ser19Cys
ENST00000611625.4:c.56C>G	ENSP00000481063.1:p.Ser19Cys
ENST00000612417.4:c.56C>G	ENSP00000478360.1:p.Ser19Cys
ENST00000621016.4:c.56C>G	ENSP00000480664.1:p.Ser19Cys
NM_004360.3:c.56C>G , LRG_301t1:c.56C>G	NP_004351.1:p.Ser19Cys
NM_001317184.1:c.56C>G	NP_001304113.1:p.Ser19Cys
NM_001317185.1:c.-1560C>G	NP_001304114.1:n.-1560C>G
NM_001317186.1:c.-1764C>G	NP_001304115.1:n.-1764C>G
NM_004360.4:c.56C>G	NP_004351.1:p.Ser19Cys
NM_004360.5:c.56C>G MANE Select	NP_004351.1:p.Ser19Cys
NM_001317184.2:c.56C>G	NP_001304113.1:p.Ser19Cys
NM_001317185.2:c.-1560C>G	NP_001304114.1:n.-1560C>G
NM_001317186.2:c.-1764C>G	NP_001304115.1:n.-1764C>G