Canonical Allele Identifier: CA2229975453

Gene: CDH1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68829944_68829959delinsTTTTTTTTTCTTTTTC , CM000678.2:g.68829944_68829959delinsTTTTTTTTTCTTTTTC	GRCh38
NC_000016.9:g.68863847_68863862delinsTTTTTTTTTCTTTTTC , CM000678.1:g.68863847_68863862delinsTTTTTTTTTCTTTTTC	GRCh37
NC_000016.8:g.67421348_67421363delinsTTTTTTTTTCTTTTTC	NCBI36
NG_008021.1:g.97653_97668delinsTTTTTTTTTCTTTTTC , LRG_301:g.97653_97668delinsTTTTTTTTTCTTTTTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261769.10:c.2439+147_2439+162delinsTTTTTTTTTCTTTTTC MANE Select	ENSP00000261769.4:n.2439+147_2439+162delinsTTTTTTTTTCTTTTTC
ENST00000261769.9:c.2439+147_2439+162delinsTTTTTTTTTCTTTTTC	ENSP00000261769.4:n.2439+147_2439+162delinsTTTTTTTTTCTTTTTC
ENST00000422392.6:c.2256+147_2256+162delinsTTTTTTTTTCTTTTTC	ENSP00000414946.2:n.2256+147_2256+162delinsTTTTTTTTTCTTTTTC
ENST00000562118.1:n.657+147_657+162delinsTTTTTTTTTCTTTTTC
ENST00000562836.5:n.2510+147_2510+162delinsTTTTTTTTTCTTTTTC
ENST00000566510.5:c.*1105+147_*1105+162delinsTTTTTTTTTCTTTTTC	ENSP00000458139.1:n.*1105+147_*1105+162delinsTTTTTTTTTCTTTTTC...
ENST00000566612.5:c.*679+147_*679+162delinsTTTTTTTTTCTTTTTC	ENSP00000454782.1:n.*679+147_*679+162delinsTTTTTTTTTCTTTTTC
ENST00000611625.4:c.2502+147_2502+162delinsTTTTTTTTTCTTTTTC	ENSP00000481063.1:n.2502+147_2502+162delinsTTTTTTTTTCTTTTTC
ENST00000612417.4:c.1853+3390_1853+3405delinsTTTTTTTTTCTTTTTC	ENSP00000478360.1:n.1853+3390_1853+3405delinsTTTTTTTTTCTTTTTC...
ENST00000621016.4:c.1866-4259_1866-4244delinsTTTTTTTTTCTTTTTC	ENSP00000480664.1:n.1866-4259_1866-4244delinsTTTTTTTTTCTTTTTC...
NM_004360.3:c.2439+147_2439+162delinsTTTTTTTTTCTTTTTC , LRG_301t1:c.2439+147_2439+162delinsTTTTTTTTTCTTTTTC	NP_004351.1:n.2439+147_2439+162delinsTTTTTTTTTCTTTTTC
XM_011523488.1:c.1704+147_1704+162delinsTTTTTTTTTCTTTTTC	XP_011521790.1:n.1704+147_1704+162delinsTTTTTTTTTCTTTTTC
XM_011523489.1:c.1704+147_1704+162delinsTTTTTTTTTCTTTTTC	XP_011521791.1:n.1704+147_1704+162delinsTTTTTTTTTCTTTTTC
NM_001317184.1:c.2256+147_2256+162delinsTTTTTTTTTCTTTTTC	NP_001304113.1:n.2256+147_2256+162delinsTTTTTTTTTCTTTTTC
NM_001317185.1:c.891+147_891+162delinsTTTTTTTTTCTTTTTC	NP_001304114.1:n.891+147_891+162delinsTTTTTTTTTCTTTTTC
NM_001317186.1:c.474+147_474+162delinsTTTTTTTTTCTTTTTC	NP_001304115.1:n.474+147_474+162delinsTTTTTTTTTCTTTTTC
NM_004360.4:c.2439+147_2439+162delinsTTTTTTTTTCTTTTTC	NP_004351.1:n.2439+147_2439+162delinsTTTTTTTTTCTTTTTC
NM_004360.5:c.2439+147_2439+162delinsTTTTTTTTTCTTTTTC MANE Select	NP_004351.1:n.2439+147_2439+162delinsTTTTTTTTTCTTTTTC
NM_001317184.2:c.2256+147_2256+162delinsTTTTTTTTTCTTTTTC	NP_001304113.1:n.2256+147_2256+162delinsTTTTTTTTTCTTTTTC
NM_001317185.2:c.891+147_891+162delinsTTTTTTTTTCTTTTTC	NP_001304114.1:n.891+147_891+162delinsTTTTTTTTTCTTTTTC
NM_001317186.2:c.474+147_474+162delinsTTTTTTTTTCTTTTTC	NP_001304115.1:n.474+147_474+162delinsTTTTTTTTTCTTTTTC