Canonical Allele Identifier: CA2229914988
Gene: CDH1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68737373A= , CM000678.2:g.68737373A= GRCh38
NC_000016.9:g.68771276A= , CM000678.1:g.68771276A= GRCh37
NC_000016.8:g.67328777A= NCBI36
NG_008021.1:g.5082A= , LRG_301:g.5082A=

Transcript Alleles

HGVS Amino-acid change
ENST00000261769.10:c.-43A= MANE Select ENSP00000261769.4:n.-43A=
ENST00000261769.9:c.-43A= ENSP00000261769.4:n.-43A=
ENST00000422392.6:c.-43A= ENSP00000414946.2:n.-43A=
ENST00000566510.5:c.-43A= ENSP00000458139.1:n.-43A=
ENST00000566612.5:c.-43A= ENSP00000454782.1:n.-43A=
ENST00000611625.4:c.-43A= ENSP00000481063.1:n.-43A=
ENST00000612417.4:c.-43A= ENSP00000478360.1:n.-43A=
ENST00000621016.4:c.-43A= ENSP00000480664.1:n.-43A=
NM_004360.3:c.-43A= , LRG_301t1:c.-43A= NP_004351.1:n.-43A=
NM_001317184.1:c.-43A= NP_001304113.1:n.-43A=
NM_001317185.1:c.-1658A= NP_001304114.1:n.-1658A=
NM_001317186.1:c.-1862A= NP_001304115.1:n.-1862A=
NM_004360.4:c.-43A= NP_004351.1:n.-43A=
NM_004360.5:c.-43A= MANE Select NP_004351.1:n.-43A=
NM_001317184.2:c.-43A= NP_001304113.1:n.-43A=
NM_001317185.2:c.-1658A= NP_001304114.1:n.-1658A=
NM_001317186.2:c.-1862A= NP_001304115.1:n.-1862A=