Canonical Allele Identifier: CA2807472300

Gene: CDH1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68810483_68810484insGG , CM000678.2:g.68810483_68810484insGG	GRCh38
NC_000016.9:g.68844386_68844387insGG , CM000678.1:g.68844386_68844387insGG	GRCh37
NC_000016.8:g.67401887_67401888insGG	NCBI36
NG_008021.1:g.78192_78193insGG , LRG_301:g.78192_78193insGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261769.10:c.832+142_832+143insGG MANE Select	ENSP00000261769.4:n.832+142_832+143insGG
ENST00000261769.9:c.832+142_832+143insGG	ENSP00000261769.4:n.832+142_832+143insGG
ENST00000422392.6:c.832+142_832+143insGG	ENSP00000414946.2:n.832+142_832+143insGG
ENST00000561751.1:c.455-1201_455-1200insGG
ENST00000562836.5:n.903+142_903+143insGG
ENST00000566510.5:c.676+142_676+143insGG	ENSP00000458139.1:n.676+142_676+143insGG
ENST00000566612.5:c.832+142_832+143insGG	ENSP00000454782.1:n.832+142_832+143insGG
ENST00000611625.4:c.832+142_832+143insGG	ENSP00000481063.1:n.832+142_832+143insGG
ENST00000612417.4:c.832+142_832+143insGG	ENSP00000478360.1:n.832+142_832+143insGG
ENST00000621016.4:c.832+142_832+143insGG	ENSP00000480664.1:n.832+142_832+143insGG
NM_004360.3:c.832+142_832+143insGG , LRG_301t1:c.832+142_832+143insGG	NP_004351.1:n.832+142_832+143insGG
XM_011523488.1:c.97+142_97+143insGG	XP_011521790.1:n.97+142_97+143insGG
XM_011523489.1:c.97+142_97+143insGG	XP_011521791.1:n.97+142_97+143insGG
NM_001317184.1:c.832+142_832+143insGG	NP_001304113.1:n.832+142_832+143insGG
NM_001317185.1:c.-784+142_-784+143insGG	NP_001304114.1:n.-784+142_-784+143insGG
NM_001317186.1:c.-988+142_-988+143insGG	NP_001304115.1:n.-988+142_-988+143insGG
NM_004360.4:c.832+142_832+143insGG	NP_004351.1:n.832+142_832+143insGG
NM_004360.5:c.832+142_832+143insGG MANE Select	NP_004351.1:n.832+142_832+143insGG
NM_001317184.2:c.832+142_832+143insGG	NP_001304113.1:n.832+142_832+143insGG
NM_001317185.2:c.-784+142_-784+143insGG	NP_001304114.1:n.-784+142_-784+143insGG
NM_001317186.2:c.-988+142_-988+143insGG	NP_001304115.1:n.-988+142_-988+143insGG