Canonical Allele Identifier: CA2229949056

Gene: CDH1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68815665_68815667delinsAAG , CM000678.2:g.68815665_68815667delinsAAG	GRCh38
NC_000016.9:g.68849568_68849570delinsAAG , CM000678.1:g.68849568_68849570delinsAAG	GRCh37
NC_000016.8:g.67407069_67407071delinsAAG	NCBI36
NG_008021.1:g.83374_83376delinsAAG , LRG_301:g.83374_83376delinsAAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261769.10:c.1471_1473delinsAAG MANE Select	ENSP00000261769.4:p.Lys491=
ENST00000261769.9:c.1471_1473delinsAAG	ENSP00000261769.4:p.Lys491=
ENST00000422392.6:c.1288_1290delinsAAG	ENSP00000414946.2:p.Lys430=
ENST00000562836.5:n.1542_1544delinsAAG
ENST00000566510.5:c.*137_*139delinsAAG	ENSP00000458139.1:n.*137_*139delinsAAG
ENST00000566612.5:c.1471_1473delinsAAG	ENSP00000454782.1:p.Lys491=
ENST00000611625.4:c.1534_1536delinsAAG	ENSP00000481063.1:p.Lys512=
ENST00000612417.4:c.1471_1473delinsAAG	ENSP00000478360.1:p.Lys491=
ENST00000621016.4:c.1471_1473delinsAAG	ENSP00000480664.1:p.Lys491=
NM_004360.3:c.1471_1473delinsAAG , LRG_301t1:c.1471_1473delinsAAG	NP_004351.1:p.Lys491=
XM_011523488.1:c.736_738delinsAAG	XP_011521790.1:p.Lys246=
XM_011523489.1:c.736_738delinsAAG	XP_011521791.1:p.Lys246=
NM_001317184.1:c.1288_1290delinsAAG	NP_001304113.1:p.Lys430=
NM_001317185.1:c.-78_-76delinsAAG	NP_001304114.1:n.-78_-76delinsAAG
NM_001317186.1:c.-349_-347delinsAAG	NP_001304115.1:n.-349_-347delinsAAG
NM_004360.4:c.1471_1473delinsAAG	NP_004351.1:p.Lys491=
NM_004360.5:c.1471_1473delinsAAG MANE Select	NP_004351.1:p.Lys491=
NM_001317184.2:c.1288_1290delinsAAG	NP_001304113.1:p.Lys430=
NM_001317185.2:c.-78_-76delinsAAG	NP_001304114.1:n.-78_-76delinsAAG
NM_001317186.2:c.-349_-347delinsAAG	NP_001304115.1:n.-349_-347delinsAAG