Canonical Allele Identifier: CA2732633092

Gene: CDH1

Linked Data

• dbSNP Id: rs1474694357

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68829875_68829876dup , CM000678.2:g.68829875_68829876dup	GRCh38
NC_000016.9:g.68863778_68863779dup , CM000678.1:g.68863778_68863779dup	GRCh37
NC_000016.8:g.67421279_67421280dup	NCBI36
NG_008021.1:g.97584_97585dup , LRG_301:g.97584_97585dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261769.10:c.2439+78_2439+79dup MANE Select	ENSP00000261769.4:n.2439+78_2439+79dup
ENST00000261769.9:c.2439+78_2439+79dup	ENSP00000261769.4:n.2439+78_2439+79dup
ENST00000422392.6:c.2256+78_2256+79dup	ENSP00000414946.2:n.2256+78_2256+79dup
ENST00000562118.1:n.657+78_657+79dup
ENST00000562836.5:n.2510+78_2510+79dup
ENST00000566510.5:c.*1105+78_*1105+79dup	ENSP00000458139.1:n.*1105+78_*1105+79dup
ENST00000566612.5:c.*679+78_*679+79dup	ENSP00000454782.1:n.*679+78_*679+79dup
ENST00000611625.4:c.2502+78_2502+79dup	ENSP00000481063.1:n.2502+78_2502+79dup
ENST00000612417.4:c.1853+3321_1853+3322dup	ENSP00000478360.1:n.1853+3321_1853+3322dup
ENST00000621016.4:c.1866-4328_1866-4327dup	ENSP00000480664.1:n.1866-4328_1866-4327dup
NM_004360.3:c.2439+78_2439+79dup , LRG_301t1:c.2439+78_2439+79dup	NP_004351.1:n.2439+78_2439+79dup
XM_011523488.1:c.1704+78_1704+79dup	XP_011521790.1:n.1704+78_1704+79dup
XM_011523489.1:c.1704+78_1704+79dup	XP_011521791.1:n.1704+78_1704+79dup
NM_001317184.1:c.2256+78_2256+79dup	NP_001304113.1:n.2256+78_2256+79dup
NM_001317185.1:c.891+78_891+79dup	NP_001304114.1:n.891+78_891+79dup
NM_001317186.1:c.474+78_474+79dup	NP_001304115.1:n.474+78_474+79dup
NM_004360.4:c.2439+78_2439+79dup	NP_004351.1:n.2439+78_2439+79dup
NM_004360.5:c.2439+78_2439+79dup MANE Select	NP_004351.1:n.2439+78_2439+79dup
NM_001317184.2:c.2256+78_2256+79dup	NP_001304113.1:n.2256+78_2256+79dup
NM_001317185.2:c.891+78_891+79dup	NP_001304114.1:n.891+78_891+79dup
NM_001317186.2:c.474+78_474+79dup	NP_001304115.1:n.474+78_474+79dup