Canonical Allele Identifier: CA283319841

Gene: CDH1

Linked Data

• dbSNP Id: rs1801026
• gnomAD v4: 16-68833553-C-A
• MyVariant Identifiers: chr16:g.68867456C>A (hg19) ; chr16:g.68833553C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68833553C>A , CM000678.2:g.68833553C>A	GRCh38
NC_000016.9:g.68867456C>A , CM000678.1:g.68867456C>A	GRCh37
NC_000016.8:g.67424957C>A	NCBI36
NG_008021.1:g.101262C>A , LRG_301:g.101262C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000261769.10:c.*54C>A MANE Select	ENSP00000261769.4:n.*54C>A
ENST00000261769.9:c.*54C>A	ENSP00000261769.4:n.*54C>A
ENST00000562118.1:n.921C>A
ENST00000566612.5:c.*943C>A	ENSP00000454782.1:n.*943C>A
ENST00000611625.4:c.*54C>A	ENSP00000481063.1:n.*54C>A
ENST00000612417.4:c.1854-638C>A	ENSP00000478360.1:n.1854-638C>A
ENST00000621016.4:c.1866-650C>A	ENSP00000480664.1:n.1866-650C>A
NM_004360.3:c.*54C>A , LRG_301t1:c.*54C>A	NP_004351.1:n.*54C>A
XM_011523488.1:c.*54C>A	XP_011521790.1:n.*54C>A
XM_011523489.1:c.*54C>A	XP_011521791.1:n.*54C>A
NM_001317184.1:c.*54C>A	NP_001304113.1:n.*54C>A
NM_001317185.1:c.*54C>A	NP_001304114.1:n.*54C>A
NM_001317186.1:c.*54C>A	NP_001304115.1:n.*54C>A
NM_004360.4:c.*54C>A	NP_004351.1:n.*54C>A
NM_004360.5:c.*54C>A MANE Select	NP_004351.1:n.*54C>A
NM_001317184.2:c.*54C>A	NP_001304113.1:n.*54C>A
NM_001317185.2:c.*54C>A	NP_001304114.1:n.*54C>A
NM_001317186.2:c.*54C>A	NP_001304115.1:n.*54C>A