Canonical Allele Identifier: CA2229982780
Gene: CDH1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68823453A= , CM000678.2:g.68823453A= GRCh38
NC_000016.9:g.68857356A= , CM000678.1:g.68857356A= GRCh37
NC_000016.8:g.67414857A= NCBI36
NG_008021.1:g.91162A= , LRG_301:g.91162A=

Transcript Alleles

HGVS Amino-acid change
ENST00000261769.10:c.1991A= MANE Select ENSP00000261769.4:p.Lys664=
ENST00000261769.9:c.1991A= ENSP00000261769.4:p.Lys664=
ENST00000422392.6:c.1808A= ENSP00000414946.2:p.Lys603=
ENST00000562118.1:n.209A=
ENST00000562836.5:n.2062A=
ENST00000566510.5:c.*657A= ENSP00000458139.1:n.*657A=
ENST00000566612.5:c.*231A= ENSP00000454782.1:n.*231A=
ENST00000611625.4:c.2054A= ENSP00000481063.1:p.Lys685=
ENST00000612417.4:c.1830+1334A= ENSP00000478360.1:n.1830+1334A=
ENST00000621016.4:c.1865+1299A= ENSP00000480664.1:n.1865+1299A=
NM_004360.3:c.1991A= , LRG_301t1:c.1991A= NP_004351.1:p.Lys664=
XM_011523488.1:c.1256A= XP_011521790.1:p.Lys419=
XM_011523489.1:c.1256A= XP_011521791.1:p.Lys419=
NM_001317184.1:c.1808A= NP_001304113.1:p.Lys603=
NM_001317185.1:c.443A= NP_001304114.1:p.Lys148=
NM_001317186.1:c.26A= NP_001304115.1:p.Lys9=
NM_004360.4:c.1991A= NP_004351.1:p.Lys664=
NM_004360.5:c.1991A= MANE Select NP_004351.1:p.Lys664=
NM_001317184.2:c.1808A= NP_001304113.1:p.Lys603=
NM_001317185.2:c.443A= NP_001304114.1:p.Lys148=
NM_001317186.2:c.26A= NP_001304115.1:p.Lys9=