Canonical Allele Identifier: CA2229982845
Gene: CDH1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68823463C= , CM000678.2:g.68823463C= GRCh38
NC_000016.9:g.68857366C= , CM000678.1:g.68857366C= GRCh37
NC_000016.8:g.67414867C= NCBI36
NG_008021.1:g.91172C= , LRG_301:g.91172C=

Transcript Alleles

HGVS Amino-acid change
ENST00000261769.10:c.2001C= MANE Select ENSP00000261769.4:p.Leu667=
ENST00000261769.9:c.2001C= ENSP00000261769.4:p.Leu667=
ENST00000422392.6:c.1818C= ENSP00000414946.2:p.Leu606=
ENST00000562118.1:n.219C=
ENST00000562836.5:n.2072C=
ENST00000566510.5:c.*667C= ENSP00000458139.1:n.*667C=
ENST00000566612.5:c.*241C= ENSP00000454782.1:n.*241C=
ENST00000611625.4:c.2064C= ENSP00000481063.1:p.Leu688=
ENST00000612417.4:c.1830+1344C= ENSP00000478360.1:n.1830+1344C=
ENST00000621016.4:c.1865+1309C= ENSP00000480664.1:n.1865+1309C=
NM_004360.3:c.2001C= , LRG_301t1:c.2001C= NP_004351.1:p.Leu667=
XM_011523488.1:c.1266C= XP_011521790.1:p.Leu422=
XM_011523489.1:c.1266C= XP_011521791.1:p.Leu422=
NM_001317184.1:c.1818C= NP_001304113.1:p.Leu606=
NM_001317185.1:c.453C= NP_001304114.1:p.Leu151=
NM_001317186.1:c.36C= NP_001304115.1:p.Leu12=
NM_004360.4:c.2001C= NP_004351.1:p.Leu667=
NM_004360.5:c.2001C= MANE Select NP_004351.1:p.Leu667=
NM_001317184.2:c.1818C= NP_001304113.1:p.Leu606=
NM_001317185.2:c.453C= NP_001304114.1:p.Leu151=
NM_001317186.2:c.36C= NP_001304115.1:p.Leu12=