Canonical Allele Identifier: CA2741495914

Gene: CDH1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68829958_68829959insTCTTTTTTTTTTTTTTT , CM000678.2:g.68829958_68829959insTCTTTTTTTTTTTTTTT	GRCh38
NC_000016.9:g.68863861_68863862insTCTTTTTTTTTTTTTTT , CM000678.1:g.68863861_68863862insTCTTTTTTTTTTTTTTT	GRCh37
NC_000016.8:g.67421362_67421363insTCTTTTTTTTTTTTTTT	NCBI36
NG_008021.1:g.97667_97668insTCTTTTTTTTTTTTTTT , LRG_301:g.97667_97668insTCTTTTTTTTTTTTTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261769.10:c.2439+161_2439+162insTCTTTTTTTTTTTTTTT MANE Select	ENSP00000261769.4:n.2439+161_2439+162insTCTTTTTTTTTTTTTTT
ENST00000261769.9:c.2439+161_2439+162insTCTTTTTTTTTTTTTTT	ENSP00000261769.4:n.2439+161_2439+162insTCTTTTTTTTTTTTTTT
ENST00000422392.6:c.2256+161_2256+162insTCTTTTTTTTTTTTTTT	ENSP00000414946.2:n.2256+161_2256+162insTCTTTTTTTTTTTTTTT
ENST00000562118.1:n.657+161_657+162insTCTTTTTTTTTTTTTTT
ENST00000562836.5:n.2510+161_2510+162insTCTTTTTTTTTTTTTTT
ENST00000566510.5:c.*1105+161_*1105+162insTCTTTTTTTTTTTTTTT	ENSP00000458139.1:n.*1105+161_*1105+162insTCTTTTTTTTTTTTTTT
ENST00000566612.5:c.*679+161_*679+162insTCTTTTTTTTTTTTTTT	ENSP00000454782.1:n.*679+161_*679+162insTCTTTTTTTTTTTTTTT
ENST00000611625.4:c.2502+161_2502+162insTCTTTTTTTTTTTTTTT	ENSP00000481063.1:n.2502+161_2502+162insTCTTTTTTTTTTTTTTT
ENST00000612417.4:c.1853+3404_1853+3405insTCTTTTTTTTTTTTTTT	ENSP00000478360.1:n.1853+3404_1853+3405insTCTTTTTTTTTTTTTTT
ENST00000621016.4:c.1866-4245_1866-4244insTCTTTTTTTTTTTTTTT	ENSP00000480664.1:n.1866-4245_1866-4244insTCTTTTTTTTTTTTTTT
NM_004360.3:c.2439+161_2439+162insTCTTTTTTTTTTTTTTT , LRG_301t1:c.2439+161_2439+162insTCTTTTTTTTTTTTTTT	NP_004351.1:n.2439+161_2439+162insTCTTTTTTTTTTTTTTT
XM_011523488.1:c.1704+161_1704+162insTCTTTTTTTTTTTTTTT	XP_011521790.1:n.1704+161_1704+162insTCTTTTTTTTTTTTTTT
XM_011523489.1:c.1704+161_1704+162insTCTTTTTTTTTTTTTTT	XP_011521791.1:n.1704+161_1704+162insTCTTTTTTTTTTTTTTT
NM_001317184.1:c.2256+161_2256+162insTCTTTTTTTTTTTTTTT	NP_001304113.1:n.2256+161_2256+162insTCTTTTTTTTTTTTTTT
NM_001317185.1:c.891+161_891+162insTCTTTTTTTTTTTTTTT	NP_001304114.1:n.891+161_891+162insTCTTTTTTTTTTTTTTT
NM_001317186.1:c.474+161_474+162insTCTTTTTTTTTTTTTTT	NP_001304115.1:n.474+161_474+162insTCTTTTTTTTTTTTTTT
NM_004360.4:c.2439+161_2439+162insTCTTTTTTTTTTTTTTT	NP_004351.1:n.2439+161_2439+162insTCTTTTTTTTTTTTTTT
NM_004360.5:c.2439+161_2439+162insTCTTTTTTTTTTTTTTT MANE Select	NP_004351.1:n.2439+161_2439+162insTCTTTTTTTTTTTTTTT
NM_001317184.2:c.2256+161_2256+162insTCTTTTTTTTTTTTTTT	NP_001304113.1:n.2256+161_2256+162insTCTTTTTTTTTTTTTTT
NM_001317185.2:c.891+161_891+162insTCTTTTTTTTTTTTTTT	NP_001304114.1:n.891+161_891+162insTCTTTTTTTTTTTTTTT
NM_001317186.2:c.474+161_474+162insTCTTTTTTTTTTTTTTT	NP_001304115.1:n.474+161_474+162insTCTTTTTTTTTTTTTTT