Canonical Allele Identifier: CA2229978306
Gene: CDH1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68833403A= , CM000678.2:g.68833403A= GRCh38
NC_000016.9:g.68867306A= , CM000678.1:g.68867306A= GRCh37
NC_000016.8:g.67424807A= NCBI36
NG_008021.1:g.101112A= , LRG_301:g.101112A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.2553A= MANE Select ENSP00000261769.4:p.Ser851=
ENST00000261769.9:c.2553A= ENSP00000261769.4:p.Ser851=
ENST00000422392.6:c.2370A= ENSP00000414946.2:p.Ser790=
ENST00000562118.1:n.771A=
ENST00000562836.5:n.2624A=
ENST00000566510.5:c.*1219A= ENSP00000458139.1:n.*1219A=
ENST00000566612.5:c.*793A= ENSP00000454782.1:n.*793A=
ENST00000611625.4:c.2616A= ENSP00000481063.1:p.Ser872=
ENST00000612417.4:c.1854-788A= ENSP00000478360.1:n.1854-788A=
ENST00000621016.4:c.1866-800A= ENSP00000480664.1:n.1866-800A=
NM_004360.3:c.2553A= , LRG_301t1:c.2553A= NP_004351.1:p.Ser851=
XM_011523488.1:c.1818A= XP_011521790.1:p.Ser606=
XM_011523489.1:c.1818A= XP_011521791.1:p.Ser606=
NM_001317184.1:c.2370A= NP_001304113.1:p.Ser790=
NM_001317185.1:c.1005A= NP_001304114.1:p.Ser335=
NM_001317186.1:c.588A= NP_001304115.1:p.Ser196=
NM_004360.4:c.2553A= NP_004351.1:p.Ser851=
NM_004360.5:c.2553A= MANE Select NP_004351.1:p.Ser851=
NM_001317184.2:c.2370A= NP_001304113.1:p.Ser790=
NM_001317185.2:c.1005A= NP_001304114.1:p.Ser335=
NM_001317186.2:c.588A= NP_001304115.1:p.Ser196=