Canonical Allele Identifier: CA2229915110
Gene: CDH1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68737416A= , CM000678.2:g.68737416A= GRCh38
NC_000016.9:g.68771319A= , CM000678.1:g.68771319A= GRCh37
NC_000016.8:g.67328820A= NCBI36
NG_008021.1:g.5125A= , LRG_301:g.5125A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.1A= MANE Select ENSP00000261769.4:p.Met1=
ENST00000261769.9:c.1A= ENSP00000261769.4:p.Met1=
ENST00000422392.6:c.1A= ENSP00000414946.2:p.Met1=
ENST00000566510.5:c.1A= ENSP00000458139.1:p.Met1=
ENST00000566612.5:c.1A= ENSP00000454782.1:p.Met1=
ENST00000611625.4:c.1A= ENSP00000481063.1:p.Met1=
ENST00000612417.4:c.1A= ENSP00000478360.1:p.Met1=
ENST00000621016.4:c.1A= ENSP00000480664.1:p.Met1=
NM_004360.3:c.1A= , LRG_301t1:c.1A= NP_004351.1:p.Met1=
NM_001317184.1:c.1A= NP_001304113.1:p.Met1=
NM_001317185.1:c.-1615A= NP_001304114.1:n.-1615A=
NM_001317186.1:c.-1819A= NP_001304115.1:n.-1819A=
NM_004360.4:c.1A= NP_004351.1:p.Met1=
NM_004360.5:c.1A= MANE Select NP_004351.1:p.Met1=
NM_001317184.2:c.1A= NP_001304113.1:p.Met1=
NM_001317185.2:c.-1615A= NP_001304114.1:n.-1615A=
NM_001317186.2:c.-1819A= NP_001304115.1:n.-1819A=