Canonical Allele Identifier: CA2229914991

Gene: CDH1

Linked Data

• dbSNP Id: rs730881658
• gnomAD v4: 16-68737375-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68737375C>G , CM000678.2:g.68737375C>G	GRCh38
NC_000016.9:g.68771278C>G , CM000678.1:g.68771278C>G	GRCh37
NC_000016.8:g.67328779C>G	NCBI36
NG_008021.1:g.5084C>G , LRG_301:g.5084C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000261769.10:c.-41C>G MANE Select	ENSP00000261769.4:n.-41C>G
ENST00000261769.9:c.-41C>G	ENSP00000261769.4:n.-41C>G
ENST00000422392.6:c.-41C>G	ENSP00000414946.2:n.-41C>G
ENST00000566510.5:c.-41C>G	ENSP00000458139.1:n.-41C>G
ENST00000566612.5:c.-41C>G	ENSP00000454782.1:n.-41C>G
ENST00000611625.4:c.-41C>G	ENSP00000481063.1:n.-41C>G
ENST00000612417.4:c.-41C>G	ENSP00000478360.1:n.-41C>G
ENST00000621016.4:c.-41C>G	ENSP00000480664.1:n.-41C>G
NM_004360.3:c.-41C>G , LRG_301t1:c.-41C>G	NP_004351.1:n.-41C>G
NM_001317184.1:c.-41C>G	NP_001304113.1:n.-41C>G
NM_001317185.1:c.-1656C>G	NP_001304114.1:n.-1656C>G
NM_001317186.1:c.-1860C>G	NP_001304115.1:n.-1860C>G
NM_004360.4:c.-41C>G	NP_004351.1:n.-41C>G
NM_004360.5:c.-41C>G MANE Select	NP_004351.1:n.-41C>G
NM_001317184.2:c.-41C>G	NP_001304113.1:n.-41C>G
NM_001317185.2:c.-1656C>G	NP_001304114.1:n.-1656C>G
NM_001317186.2:c.-1860C>G	NP_001304115.1:n.-1860C>G