Canonical Allele Identifier: CA2229975670
Gene: CDH1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68830025T= , CM000678.2:g.68830025T= GRCh38
NC_000016.9:g.68863928T= , CM000678.1:g.68863928T= GRCh37
NC_000016.8:g.67421429T= NCBI36
NG_008021.1:g.97734T= , LRG_301:g.97734T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.2439+228T= MANE Select ENSP00000261769.4:n.2439+228T=
ENST00000261769.9:c.2439+228T= ENSP00000261769.4:n.2439+228T=
ENST00000422392.6:c.2256+228T= ENSP00000414946.2:n.2256+228T=
ENST00000562118.1:n.657+228T=
ENST00000562836.5:n.2510+228T=
ENST00000566510.5:c.*1105+228T= ENSP00000458139.1:n.*1105+228T=
ENST00000566612.5:c.*679+228T= ENSP00000454782.1:n.*679+228T=
ENST00000611625.4:c.2502+228T= ENSP00000481063.1:n.2502+228T=
ENST00000612417.4:c.1853+3471T= ENSP00000478360.1:n.1853+3471T=
ENST00000621016.4:c.1866-4178T= ENSP00000480664.1:n.1866-4178T=
NM_004360.3:c.2439+228T= , LRG_301t1:c.2439+228T= NP_004351.1:n.2439+228T=
XM_011523488.1:c.1704+228T= XP_011521790.1:n.1704+228T=
XM_011523489.1:c.1704+228T= XP_011521791.1:n.1704+228T=
NM_001317184.1:c.2256+228T= NP_001304113.1:n.2256+228T=
NM_001317185.1:c.891+228T= NP_001304114.1:n.891+228T=
NM_001317186.1:c.474+228T= NP_001304115.1:n.474+228T=
NM_004360.4:c.2439+228T= NP_004351.1:n.2439+228T=
NM_004360.5:c.2439+228T= MANE Select NP_004351.1:n.2439+228T=
NM_001317184.2:c.2256+228T= NP_001304113.1:n.2256+228T=
NM_001317185.2:c.891+228T= NP_001304114.1:n.891+228T=
NM_001317186.2:c.474+228T= NP_001304115.1:n.474+228T=