Canonical Allele Identifier: CA283273142

Gene: CDH1

Linked Data

• dbSNP Id: rs893677325
• gnomAD v4: 16-68737297-C-A
• MyVariant Identifiers: chr16:g.68771200C>A (hg19) ; chr16:g.68737297C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68737297C>A , CM000678.2:g.68737297C>A	GRCh38
NC_000016.9:g.68771200C>A , CM000678.1:g.68771200C>A	GRCh37
NC_000016.8:g.67328701C>A	NCBI36
NG_008021.1:g.5006C>A , LRG_301:g.5006C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000261769.10:c.-119C>A MANE Select	ENSP00000261769.4:n.-119C>A
ENST00000261769.9:c.-119C>A	ENSP00000261769.4:n.-119C>A
ENST00000611625.4:c.-119C>A	ENSP00000481063.1:n.-119C>A
ENST00000612417.4:c.-119C>A	ENSP00000478360.1:n.-119C>A
NM_004360.3:c.-119C>A , LRG_301t1:c.-119C>A	NP_004351.1:n.-119C>A
NM_001317184.1:c.-119C>A	NP_001304113.1:n.-119C>A
NM_001317185.1:c.-1734C>A	NP_001304114.1:n.-1734C>A
NM_001317186.1:c.-1938C>A	NP_001304115.1:n.-1938C>A
NM_004360.4:c.-119C>A	NP_004351.1:n.-119C>A
NM_004360.5:c.-119C>A MANE Select	NP_004351.1:n.-119C>A
NM_001317184.2:c.-119C>A	NP_001304113.1:n.-119C>A
NM_001317185.2:c.-1734C>A	NP_001304114.1:n.-1734C>A
NM_001317186.2:c.-1938C>A	NP_001304115.1:n.-1938C>A