Canonical Allele Identifier: CA2229914989
Gene: CDH1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68737374C= , CM000678.2:g.68737374C= GRCh38
NC_000016.9:g.68771277C= , CM000678.1:g.68771277C= GRCh37
NC_000016.8:g.67328778C= NCBI36
NG_008021.1:g.5083C= , LRG_301:g.5083C=

Transcript Alleles

HGVS Amino-acid change
ENST00000261769.10:c.-42C= MANE Select ENSP00000261769.4:n.-42C=
ENST00000261769.9:c.-42C= ENSP00000261769.4:n.-42C=
ENST00000422392.6:c.-42C= ENSP00000414946.2:n.-42C=
ENST00000566510.5:c.-42C= ENSP00000458139.1:n.-42C=
ENST00000566612.5:c.-42C= ENSP00000454782.1:n.-42C=
ENST00000611625.4:c.-42C= ENSP00000481063.1:n.-42C=
ENST00000612417.4:c.-42C= ENSP00000478360.1:n.-42C=
ENST00000621016.4:c.-42C= ENSP00000480664.1:n.-42C=
NM_004360.3:c.-42C= , LRG_301t1:c.-42C= NP_004351.1:n.-42C=
NM_001317184.1:c.-42C= NP_001304113.1:n.-42C=
NM_001317185.1:c.-1657C= NP_001304114.1:n.-1657C=
NM_001317186.1:c.-1861C= NP_001304115.1:n.-1861C=
NM_004360.4:c.-42C= NP_004351.1:n.-42C=
NM_004360.5:c.-42C= MANE Select NP_004351.1:n.-42C=
NM_001317184.2:c.-42C= NP_001304113.1:n.-42C=
NM_001317185.2:c.-1657C= NP_001304114.1:n.-1657C=
NM_001317186.2:c.-1861C= NP_001304115.1:n.-1861C=