Canonical Allele Identifier: CA283273170

Gene: CDH1

Linked Data

• dbSNP Id: rs574467384
• gnomAD v3: 16-68737305-C-G
• gnomAD v4: 16-68737305-C-G
• MyVariant Identifiers: chr16:g.68771208C>G (hg19) ; chr16:g.68737305C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68737305C>G , CM000678.2:g.68737305C>G	GRCh38
NC_000016.9:g.68771208C>G , CM000678.1:g.68771208C>G	GRCh37
NC_000016.8:g.67328709C>G	NCBI36
NG_008021.1:g.5014C>G , LRG_301:g.5014C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000261769.10:c.-111C>G MANE Select	ENSP00000261769.4:n.-111C>G
ENST00000261769.9:c.-111C>G	ENSP00000261769.4:n.-111C>G
ENST00000611625.4:c.-111C>G	ENSP00000481063.1:n.-111C>G
ENST00000612417.4:c.-111C>G	ENSP00000478360.1:n.-111C>G
NM_004360.3:c.-111C>G , LRG_301t1:c.-111C>G	NP_004351.1:n.-111C>G
NM_001317184.1:c.-111C>G	NP_001304113.1:n.-111C>G
NM_001317185.1:c.-1726C>G	NP_001304114.1:n.-1726C>G
NM_001317186.1:c.-1930C>G	NP_001304115.1:n.-1930C>G
NM_004360.4:c.-111C>G	NP_004351.1:n.-111C>G
NM_004360.5:c.-111C>G MANE Select	NP_004351.1:n.-111C>G
NM_001317184.2:c.-111C>G	NP_001304113.1:n.-111C>G
NM_001317185.2:c.-1726C>G	NP_001304114.1:n.-1726C>G
NM_001317186.2:c.-1930C>G	NP_001304115.1:n.-1930C>G