Canonical Allele Identifier: CA2229948422
Gene: CDH1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68815570T= , CM000678.2:g.68815570T= GRCh38
NC_000016.9:g.68849473T= , CM000678.1:g.68849473T= GRCh37
NC_000016.8:g.67406974T= NCBI36
NG_008021.1:g.83279T= , LRG_301:g.83279T=

Transcript Alleles

HGVS Amino-acid change
ENST00000261769.10:c.1376T= MANE Select ENSP00000261769.4:p.Val459=
ENST00000261769.9:c.1376T= ENSP00000261769.4:p.Val459=
ENST00000422392.6:c.1193T= ENSP00000414946.2:p.Val398=
ENST00000562836.5:n.1447T=
ENST00000566510.5:c.*42T= ENSP00000458139.1:n.*42T=
ENST00000566612.5:c.1376T= ENSP00000454782.1:p.Val459=
ENST00000611625.4:c.1439T= ENSP00000481063.1:p.Val480=
ENST00000612417.4:c.1376T= ENSP00000478360.1:p.Val459=
ENST00000621016.4:c.1376T= ENSP00000480664.1:p.Val459=
NM_004360.3:c.1376T= , LRG_301t1:c.1376T= NP_004351.1:p.Val459=
XM_011523488.1:c.641T= XP_011521790.1:p.Val214=
XM_011523489.1:c.641T= XP_011521791.1:p.Val214=
NM_001317184.1:c.1193T= NP_001304113.1:p.Val398=
NM_001317185.1:c.-173T= NP_001304114.1:n.-173T=
NM_001317186.1:c.-444T= NP_001304115.1:n.-444T=
NM_004360.4:c.1376T= NP_004351.1:p.Val459=
NM_004360.5:c.1376T= MANE Select NP_004351.1:p.Val459=
NM_001317184.2:c.1193T= NP_001304113.1:p.Val398=
NM_001317185.2:c.-173T= NP_001304114.1:n.-173T=
NM_001317186.2:c.-444T= NP_001304115.1:n.-444T=