Canonical Allele Identifier: CA396467038

Gene: CDH1

Linked Data

• ClinVar Variation Id: 2880910
• ClinVar RCV Id: RCV003624061
• dbSNP Id: rs786201888
• MyVariant Identifiers: chr16:g.68856050C>G (hg19) ; chr16:g.68822147C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68822147C>G , CM000678.2:g.68822147C>G	GRCh38
NC_000016.9:g.68856050C>G , CM000678.1:g.68856050C>G	GRCh37
NC_000016.8:g.67413551C>G	NCBI36
NG_008021.1:g.89856C>G , LRG_301:g.89856C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000261769.10:c.1858C>G MANE Select	ENSP00000261769.4:p.Pro620Ala
ENST00000261769.9:c.1858C>G	ENSP00000261769.4:p.Pro620Ala
ENST00000422392.6:c.1675C>G	ENSP00000414946.2:p.Pro559Ala
ENST00000562836.5:n.1929C>G
ENST00000566510.5:c.*524C>G	ENSP00000458139.1:n.*524C>G
ENST00000566612.5:c.*98C>G	ENSP00000454782.1:n.*98C>G
ENST00000611625.4:c.1921C>G	ENSP00000481063.1:p.Pro641Ala
ENST00000612417.4:c.1830+28C>G	ENSP00000478360.1:n.1830+28C>G
ENST00000621016.4:c.1858C>G	ENSP00000480664.1:p.Pro620Ala
NM_004360.3:c.1858C>G , LRG_301t1:c.1858C>G	NP_004351.1:p.Pro620Ala
XM_011523488.1:c.1123C>G	XP_011521790.1:p.Pro375Ala
XM_011523489.1:c.1123C>G	XP_011521791.1:p.Pro375Ala
NM_001317184.1:c.1675C>G	NP_001304113.1:p.Pro559Ala
NM_001317185.1:c.310C>G	NP_001304114.1:p.Pro104Ala
NM_001317186.1:c.-108C>G	NP_001304115.1:n.-108C>G
NM_004360.4:c.1858C>G	NP_004351.1:p.Pro620Ala
NM_004360.5:c.1858C>G MANE Select	NP_004351.1:p.Pro620Ala
NM_001317184.2:c.1675C>G	NP_001304113.1:p.Pro559Ala
NM_001317185.2:c.310C>G	NP_001304114.1:p.Pro104Ala
NM_001317186.2:c.-108C>G	NP_001304115.1:n.-108C>G