Canonical Allele Identifier: CA3000999149

Gene: CDH1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68737363dup , CM000678.2:g.68737363dup	GRCh38
NC_000016.9:g.68771266dup , CM000678.1:g.68771266dup	GRCh37
NC_000016.8:g.67328767dup	NCBI36
NG_008021.1:g.5072dup , LRG_301:g.5072dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261769.10:c.-53dup MANE Select	ENSP00000261769.4:n.-53dup
ENST00000261769.9:c.-53dup	ENSP00000261769.4:n.-53dup
ENST00000422392.6:c.-53dup	ENSP00000414946.2:n.-53dup
ENST00000566510.5:c.-53dup	ENSP00000458139.1:n.-53dup
ENST00000566612.5:c.-53dup	ENSP00000454782.1:n.-53dup
ENST00000611625.4:c.-53dup	ENSP00000481063.1:n.-53dup
ENST00000612417.4:c.-53dup	ENSP00000478360.1:n.-53dup
ENST00000621016.4:c.-53dup	ENSP00000480664.1:n.-53dup
NM_004360.3:c.-53dup , LRG_301t1:c.-53dup	NP_004351.1:n.-53dup
NM_001317184.1:c.-53dup	NP_001304113.1:n.-53dup
NM_001317185.1:c.-1668dup	NP_001304114.1:n.-1668dup
NM_001317186.1:c.-1872dup	NP_001304115.1:n.-1872dup
NM_004360.4:c.-53dup	NP_004351.1:n.-53dup
NM_004360.5:c.-53dup MANE Select	NP_004351.1:n.-53dup
NM_001317184.2:c.-53dup	NP_001304113.1:n.-53dup
NM_001317185.2:c.-1668dup	NP_001304114.1:n.-1668dup
NM_001317186.2:c.-1872dup	NP_001304115.1:n.-1872dup