Canonical Allele Identifier: CA2229975582

Gene: CDH1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68829967_68829975delinsTTTTTTTTG , CM000678.2:g.68829967_68829975delinsTTTTTTTTG	GRCh38
NC_000016.9:g.68863870_68863878delinsTTTTTTTTG , CM000678.1:g.68863870_68863878delinsTTTTTTTTG	GRCh37
NC_000016.8:g.67421371_67421379delinsTTTTTTTTG	NCBI36
NG_008021.1:g.97676_97684delinsTTTTTTTTG , LRG_301:g.97676_97684delinsTTTTTTTTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261769.10:c.2439+170_2439+178delinsTTTTTTTTG MANE Select	ENSP00000261769.4:n.2439+170_2439+178delinsTTTTTTTTG
ENST00000261769.9:c.2439+170_2439+178delinsTTTTTTTTG	ENSP00000261769.4:n.2439+170_2439+178delinsTTTTTTTTG
ENST00000422392.6:c.2256+170_2256+178delinsTTTTTTTTG	ENSP00000414946.2:n.2256+170_2256+178delinsTTTTTTTTG
ENST00000562118.1:n.657+170_657+178delinsTTTTTTTTG
ENST00000562836.5:n.2510+170_2510+178delinsTTTTTTTTG
ENST00000566510.5:c.*1105+170_*1105+178delinsTTTTTTTTG	ENSP00000458139.1:n.*1105+170_*1105+178delinsTTTTTTTTG
ENST00000566612.5:c.*679+170_*679+178delinsTTTTTTTTG	ENSP00000454782.1:n.*679+170_*679+178delinsTTTTTTTTG
ENST00000611625.4:c.2502+170_2502+178delinsTTTTTTTTG	ENSP00000481063.1:n.2502+170_2502+178delinsTTTTTTTTG
ENST00000612417.4:c.1853+3413_1853+3421delinsTTTTTTTTG	ENSP00000478360.1:n.1853+3413_1853+3421delinsTTTTTTTTG
ENST00000621016.4:c.1866-4236_1866-4228delinsTTTTTTTTG	ENSP00000480664.1:n.1866-4236_1866-4228delinsTTTTTTTTG
NM_004360.3:c.2439+170_2439+178delinsTTTTTTTTG , LRG_301t1:c.2439+170_2439+178delinsTTTTTTTTG	NP_004351.1:n.2439+170_2439+178delinsTTTTTTTTG
XM_011523488.1:c.1704+170_1704+178delinsTTTTTTTTG	XP_011521790.1:n.1704+170_1704+178delinsTTTTTTTTG
XM_011523489.1:c.1704+170_1704+178delinsTTTTTTTTG	XP_011521791.1:n.1704+170_1704+178delinsTTTTTTTTG
NM_001317184.1:c.2256+170_2256+178delinsTTTTTTTTG	NP_001304113.1:n.2256+170_2256+178delinsTTTTTTTTG
NM_001317185.1:c.891+170_891+178delinsTTTTTTTTG	NP_001304114.1:n.891+170_891+178delinsTTTTTTTTG
NM_001317186.1:c.474+170_474+178delinsTTTTTTTTG	NP_001304115.1:n.474+170_474+178delinsTTTTTTTTG
NM_004360.4:c.2439+170_2439+178delinsTTTTTTTTG	NP_004351.1:n.2439+170_2439+178delinsTTTTTTTTG
NM_004360.5:c.2439+170_2439+178delinsTTTTTTTTG MANE Select	NP_004351.1:n.2439+170_2439+178delinsTTTTTTTTG
NM_001317184.2:c.2256+170_2256+178delinsTTTTTTTTG	NP_001304113.1:n.2256+170_2256+178delinsTTTTTTTTG
NM_001317185.2:c.891+170_891+178delinsTTTTTTTTG	NP_001304114.1:n.891+170_891+178delinsTTTTTTTTG
NM_001317186.2:c.474+170_474+178delinsTTTTTTTTG	NP_001304115.1:n.474+170_474+178delinsTTTTTTTTG