Canonical Allele Identifier: CA396472655
Gene: CDH1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68833451T>A , CM000678.2:g.68833451T>A GRCh38
NC_000016.9:g.68867354T>A , CM000678.1:g.68867354T>A GRCh37
NC_000016.8:g.67424855T>A NCBI36
NG_008021.1:g.101160T>A , LRG_301:g.101160T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.2601T>A MANE Select ENSP00000261769.4:p.Asn867Lys
ENST00000261769.9:c.2601T>A ENSP00000261769.4:p.Asn867Lys
ENST00000422392.6:c.2418T>A ENSP00000414946.2:p.Asn806Lys
ENST00000562118.1:n.819T>A
ENST00000562836.5:n.2672T>A
ENST00000566510.5:c.*1267T>A ENSP00000458139.1:n.*1267T>A
ENST00000566612.5:c.*841T>A ENSP00000454782.1:n.*841T>A
ENST00000611625.4:c.2664T>A ENSP00000481063.1:p.Asn888Lys
ENST00000612417.4:c.1854-740T>A ENSP00000478360.1:n.1854-740T>A
ENST00000621016.4:c.1866-752T>A ENSP00000480664.1:n.1866-752T>A
NM_004360.3:c.2601T>A , LRG_301t1:c.2601T>A NP_004351.1:p.Asn867Lys
XM_011523488.1:c.1866T>A XP_011521790.1:p.Asn622Lys
XM_011523489.1:c.1866T>A XP_011521791.1:p.Asn622Lys
NM_001317184.1:c.2418T>A NP_001304113.1:p.Asn806Lys
NM_001317185.1:c.1053T>A NP_001304114.1:p.Asn351Lys
NM_001317186.1:c.636T>A NP_001304115.1:p.Asn212Lys
NM_004360.4:c.2601T>A NP_004351.1:p.Asn867Lys
NM_004360.5:c.2601T>A MANE Select NP_004351.1:p.Asn867Lys
NM_001317184.2:c.2418T>A NP_001304113.1:p.Asn806Lys
NM_001317185.2:c.1053T>A NP_001304114.1:p.Asn351Lys
NM_001317186.2:c.636T>A NP_001304115.1:p.Asn212Lys