Canonical Allele Identifier: CA2229975232
Gene: CDH1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68829789A= , CM000678.2:g.68829789A= GRCh38
NC_000016.9:g.68863692A= , CM000678.1:g.68863692A= GRCh37
NC_000016.8:g.67421193A= NCBI36
NG_008021.1:g.97498A= , LRG_301:g.97498A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.2431A= MANE Select ENSP00000261769.4:p.Ile811=
ENST00000261769.9:c.2431A= ENSP00000261769.4:p.Ile811=
ENST00000422392.6:c.2248A= ENSP00000414946.2:p.Ile750=
ENST00000562118.1:n.649A=
ENST00000562836.5:n.2502A=
ENST00000566510.5:c.*1097A= ENSP00000458139.1:n.*1097A=
ENST00000566612.5:c.*671A= ENSP00000454782.1:n.*671A=
ENST00000611625.4:c.2494A= ENSP00000481063.1:p.Ile832=
ENST00000612417.4:c.1853+3235A= ENSP00000478360.1:n.1853+3235A=
ENST00000621016.4:c.1866-4414A= ENSP00000480664.1:n.1866-4414A=
NM_004360.3:c.2431A= , LRG_301t1:c.2431A= NP_004351.1:p.Ile811=
XM_011523488.1:c.1696A= XP_011521790.1:p.Ile566=
XM_011523489.1:c.1696A= XP_011521791.1:p.Ile566=
NM_001317184.1:c.2248A= NP_001304113.1:p.Ile750=
NM_001317185.1:c.883A= NP_001304114.1:p.Ile295=
NM_001317186.1:c.466A= NP_001304115.1:p.Ile156=
NM_004360.4:c.2431A= NP_004351.1:p.Ile811=
NM_004360.5:c.2431A= MANE Select NP_004351.1:p.Ile811=
NM_001317184.2:c.2248A= NP_001304113.1:p.Ile750=
NM_001317185.2:c.883A= NP_001304114.1:p.Ile295=
NM_001317186.2:c.466A= NP_001304115.1:p.Ile156=