Canonical Allele Identifier: CA396464836
Gene: CDH1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr16:g.68853192T>G (hg19) chr16:g.68819289T>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68819289T>G , CM000678.2:g.68819289T>G GRCh38
NC_000016.9:g.68853192T>G , CM000678.1:g.68853192T>G GRCh37
NC_000016.8:g.67410693T>G NCBI36
NG_008021.1:g.86998T>G , LRG_301:g.86998T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.1575T>G MANE Select ENSP00000261769.4:p.Ile525Met
ENST00000261769.9:c.1575T>G ENSP00000261769.4:p.Ile525Met
ENST00000422392.6:c.1392T>G ENSP00000414946.2:p.Ile464Met
ENST00000562836.5:n.1646T>G
ENST00000566510.5:c.*241T>G ENSP00000458139.1:n.*241T>G
ENST00000566612.5:c.1566-2712T>G ENSP00000454782.1:n.1566-2712T>G
ENST00000611625.4:c.1638T>G ENSP00000481063.1:p.Ile546Met
ENST00000612417.4:c.1575T>G ENSP00000478360.1:p.Ile525Met
ENST00000621016.4:c.1575T>G ENSP00000480664.1:p.Ile525Met
NM_004360.3:c.1575T>G , LRG_301t1:c.1575T>G NP_004351.1:p.Ile525Met
XM_011523488.1:c.840T>G XP_011521790.1:p.Ile280Met
XM_011523489.1:c.840T>G XP_011521791.1:p.Ile280Met
NM_001317184.1:c.1392T>G NP_001304113.1:p.Ile464Met
NM_001317185.1:c.27T>G NP_001304114.1:p.Ile9Met
NM_001317186.1:c.-254-2712T>G NP_001304115.1:n.-254-2712T>G
NM_004360.4:c.1575T>G NP_004351.1:p.Ile525Met
NM_004360.5:c.1575T>G MANE Select NP_004351.1:p.Ile525Met
NM_001317184.2:c.1392T>G NP_001304113.1:p.Ile464Met
NM_001317185.2:c.27T>G NP_001304114.1:p.Ile9Met
NM_001317186.2:c.-254-2712T>G NP_001304115.1:n.-254-2712T>G
Search 100 bp 5'
Search 100 bp 3'