Canonical Allele Identifier: CA2229978028
Gene: CDH1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68833192G= , CM000678.2:g.68833192G= GRCh38
NC_000016.9:g.68867095G= , CM000678.1:g.68867095G= GRCh37
NC_000016.8:g.67424596G= NCBI36
NG_008021.1:g.100901G= , LRG_301:g.100901G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.2440-98G= MANE Select ENSP00000261769.4:n.2440-98G=
ENST00000261769.9:c.2440-98G= ENSP00000261769.4:n.2440-98G=
ENST00000422392.6:c.2257-98G= ENSP00000414946.2:n.2257-98G=
ENST00000562118.1:n.658-98G=
ENST00000562836.5:n.2511-98G=
ENST00000566510.5:c.*1106-98G= ENSP00000458139.1:n.*1106-98G=
ENST00000566612.5:c.*680-98G= ENSP00000454782.1:n.*680-98G=
ENST00000611625.4:c.2503-98G= ENSP00000481063.1:n.2503-98G=
ENST00000612417.4:c.1854-999G= ENSP00000478360.1:n.1854-999G=
ENST00000621016.4:c.1866-1011G= ENSP00000480664.1:n.1866-1011G=
NM_004360.3:c.2440-98G= , LRG_301t1:c.2440-98G= NP_004351.1:n.2440-98G=
XM_011523488.1:c.1705-98G= XP_011521790.1:n.1705-98G=
XM_011523489.1:c.1705-98G= XP_011521791.1:n.1705-98G=
NM_001317184.1:c.2257-98G= NP_001304113.1:n.2257-98G=
NM_001317185.1:c.892-98G= NP_001304114.1:n.892-98G=
NM_001317186.1:c.475-98G= NP_001304115.1:n.475-98G=
NM_004360.4:c.2440-98G= NP_004351.1:n.2440-98G=
NM_004360.5:c.2440-98G= MANE Select NP_004351.1:n.2440-98G=
NM_001317184.2:c.2257-98G= NP_001304113.1:n.2257-98G=
NM_001317185.2:c.892-98G= NP_001304114.1:n.892-98G=
NM_001317186.2:c.475-98G= NP_001304115.1:n.475-98G=