Canonical Allele Identifier: CA2229915309
Gene: CDH1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68737457G= , CM000678.2:g.68737457G= GRCh38
NC_000016.9:g.68771360G= , CM000678.1:g.68771360G= GRCh37
NC_000016.8:g.67328861G= NCBI36
NG_008021.1:g.5166G= , LRG_301:g.5166G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.42G= MANE Select ENSP00000261769.4:p.Leu14=
ENST00000261769.9:c.42G= ENSP00000261769.4:p.Leu14=
ENST00000422392.6:c.42G= ENSP00000414946.2:p.Leu14=
ENST00000566510.5:c.42G= ENSP00000458139.1:p.Leu14=
ENST00000566612.5:c.42G= ENSP00000454782.1:p.Leu14=
ENST00000611625.4:c.42G= ENSP00000481063.1:p.Leu14=
ENST00000612417.4:c.42G= ENSP00000478360.1:p.Leu14=
ENST00000621016.4:c.42G= ENSP00000480664.1:p.Leu14=
NM_004360.3:c.42G= , LRG_301t1:c.42G= NP_004351.1:p.Leu14=
NM_001317184.1:c.42G= NP_001304113.1:p.Leu14=
NM_001317185.1:c.-1574G= NP_001304114.1:n.-1574G=
NM_001317186.1:c.-1778G= NP_001304115.1:n.-1778G=
NM_004360.4:c.42G= NP_004351.1:p.Leu14=
NM_004360.5:c.42G= MANE Select NP_004351.1:p.Leu14=
NM_001317184.2:c.42G= NP_001304113.1:p.Leu14=
NM_001317185.2:c.-1574G= NP_001304114.1:n.-1574G=
NM_001317186.2:c.-1778G= NP_001304115.1:n.-1778G=