Canonical Allele Identifier: CA913188705

Gene: CDH1

Linked Data

• ClinVar Variation Id: 3076086
• ClinVar RCV Id: RCV004018403
• dbSNP Id: rs1962421473
• gnomAD v3: 16-68737396-C-T
• gnomAD v4: 16-68737396-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68737396C>T , CM000678.2:g.68737396C>T	GRCh38
NC_000016.9:g.68771299C>T , CM000678.1:g.68771299C>T	GRCh37
NC_000016.8:g.67328800C>T	NCBI36
NG_008021.1:g.5105C>T , LRG_301:g.5105C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261769.10:c.-20C>T MANE Select	ENSP00000261769.4:n.-20C>T
ENST00000261769.9:c.-20C>T	ENSP00000261769.4:n.-20C>T
ENST00000422392.6:c.-20C>T	ENSP00000414946.2:n.-20C>T
ENST00000566510.5:c.-20C>T	ENSP00000458139.1:n.-20C>T
ENST00000566612.5:c.-20C>T	ENSP00000454782.1:n.-20C>T
ENST00000611625.4:c.-20C>T	ENSP00000481063.1:n.-20C>T
ENST00000612417.4:c.-20C>T	ENSP00000478360.1:n.-20C>T
ENST00000621016.4:c.-20C>T	ENSP00000480664.1:n.-20C>T
NM_004360.3:c.-20C>T , LRG_301t1:c.-20C>T	NP_004351.1:n.-20C>T
NM_001317184.1:c.-20C>T	NP_001304113.1:n.-20C>T
NM_001317185.1:c.-1635C>T	NP_001304114.1:n.-1635C>T
NM_001317186.1:c.-1839C>T	NP_001304115.1:n.-1839C>T
NM_004360.4:c.-20C>T	NP_004351.1:n.-20C>T
NM_004360.5:c.-20C>T MANE Select	NP_004351.1:n.-20C>T
NM_001317184.2:c.-20C>T	NP_001304113.1:n.-20C>T
NM_001317185.2:c.-1635C>T	NP_001304114.1:n.-1635C>T
NM_001317186.2:c.-1839C>T	NP_001304115.1:n.-1839C>T