Canonical Allele Identifier: CA2576038894
Gene: CDH1 HGNC NCBI

Linked Data

dbSNP Id: rs2152142585

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68829873A>G , CM000678.2:g.68829873A>G GRCh38
NC_000016.9:g.68863776A>G , CM000678.1:g.68863776A>G GRCh37
NC_000016.8:g.67421277A>G NCBI36
NG_008021.1:g.97582A>G , LRG_301:g.97582A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.2439+76A>G MANE Select ENSP00000261769.4:n.2439+76A>G
ENST00000261769.9:c.2439+76A>G ENSP00000261769.4:n.2439+76A>G
ENST00000422392.6:c.2256+76A>G ENSP00000414946.2:n.2256+76A>G
ENST00000562118.1:n.657+76A>G
ENST00000562836.5:n.2510+76A>G
ENST00000566510.5:c.*1105+76A>G ENSP00000458139.1:n.*1105+76A>G
ENST00000566612.5:c.*679+76A>G ENSP00000454782.1:n.*679+76A>G
ENST00000611625.4:c.2502+76A>G ENSP00000481063.1:n.2502+76A>G
ENST00000612417.4:c.1853+3319A>G ENSP00000478360.1:n.1853+3319A>G
ENST00000621016.4:c.1866-4330A>G ENSP00000480664.1:n.1866-4330A>G
NM_004360.3:c.2439+76A>G , LRG_301t1:c.2439+76A>G NP_004351.1:n.2439+76A>G
XM_011523488.1:c.1704+76A>G XP_011521790.1:n.1704+76A>G
XM_011523489.1:c.1704+76A>G XP_011521791.1:n.1704+76A>G
NM_001317184.1:c.2256+76A>G NP_001304113.1:n.2256+76A>G
NM_001317185.1:c.891+76A>G NP_001304114.1:n.891+76A>G
NM_001317186.1:c.474+76A>G NP_001304115.1:n.474+76A>G
NM_004360.4:c.2439+76A>G NP_004351.1:n.2439+76A>G
NM_004360.5:c.2439+76A>G MANE Select NP_004351.1:n.2439+76A>G
NM_001317184.2:c.2256+76A>G NP_001304113.1:n.2256+76A>G
NM_001317185.2:c.891+76A>G NP_001304114.1:n.891+76A>G
NM_001317186.2:c.474+76A>G NP_001304115.1:n.474+76A>G