Canonical Allele Identifier: CA2633933494

Gene: CDH1

Linked Data

• gnomAD v4: 16-68834634-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68834634C>A , CM000678.2:g.68834634C>A	GRCh38
NC_000016.9:g.68868537C>A , CM000678.1:g.68868537C>A	GRCh37
NC_000016.8:g.67426038C>A	NCBI36
NG_008021.1:g.102343C>A , LRG_301:g.102343C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000261769.10:c.*1135C>A MANE Select	ENSP00000261769.4:n.*1135C>A
ENST00000261769.9:c.*1135C>A	ENSP00000261769.4:n.*1135C>A
ENST00000566612.5:c.*2024C>A	ENSP00000454782.1:n.*2024C>A
ENST00000611625.4:c.*1135C>A	ENSP00000481063.1:n.*1135C>A
ENST00000621016.4:c.*353C>A	ENSP00000480664.1:n.*353C>A
NM_004360.3:c.*1135C>A , LRG_301t1:c.*1135C>A	NP_004351.1:n.*1135C>A
XM_011523488.1:c.*1135C>A	XP_011521790.1:n.*1135C>A
XM_011523489.1:c.*1135C>A	XP_011521791.1:n.*1135C>A
NM_001317184.1:c.*1135C>A	NP_001304113.1:n.*1135C>A
NM_001317185.1:c.*1135C>A	NP_001304114.1:n.*1135C>A
NM_001317186.1:c.*1135C>A	NP_001304115.1:n.*1135C>A
NM_004360.4:c.*1135C>A	NP_004351.1:n.*1135C>A
NM_004360.5:c.*1135C>A MANE Select	NP_004351.1:n.*1135C>A
NM_001317184.2:c.*1135C>A	NP_001304113.1:n.*1135C>A
NM_001317185.2:c.*1135C>A	NP_001304114.1:n.*1135C>A
NM_001317186.2:c.*1135C>A	NP_001304115.1:n.*1135C>A