Canonical Allele Identifier: CA2732921287

Gene: CDH1

Linked Data

• dbSNP Id: rs2152142497

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68829805A>T , CM000678.2:g.68829805A>T	GRCh38
NC_000016.9:g.68863708A>T , CM000678.1:g.68863708A>T	GRCh37
NC_000016.8:g.67421209A>T	NCBI36
NG_008021.1:g.97514A>T , LRG_301:g.97514A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261769.10:c.2439+8A>T MANE Select	ENSP00000261769.4:n.2439+8A>T
ENST00000261769.9:c.2439+8A>T	ENSP00000261769.4:n.2439+8A>T
ENST00000422392.6:c.2256+8A>T	ENSP00000414946.2:n.2256+8A>T
ENST00000562118.1:n.657+8A>T
ENST00000562836.5:n.2510+8A>T
ENST00000566510.5:c.*1105+8A>T	ENSP00000458139.1:n.*1105+8A>T
ENST00000566612.5:c.*679+8A>T	ENSP00000454782.1:n.*679+8A>T
ENST00000611625.4:c.2502+8A>T	ENSP00000481063.1:n.2502+8A>T
ENST00000612417.4:c.1853+3251A>T	ENSP00000478360.1:n.1853+3251A>T
ENST00000621016.4:c.1866-4398A>T	ENSP00000480664.1:n.1866-4398A>T
NM_004360.3:c.2439+8A>T , LRG_301t1:c.2439+8A>T	NP_004351.1:n.2439+8A>T
XM_011523488.1:c.1704+8A>T	XP_011521790.1:n.1704+8A>T
XM_011523489.1:c.1704+8A>T	XP_011521791.1:n.1704+8A>T
NM_001317184.1:c.2256+8A>T	NP_001304113.1:n.2256+8A>T
NM_001317185.1:c.891+8A>T	NP_001304114.1:n.891+8A>T
NM_001317186.1:c.474+8A>T	NP_001304115.1:n.474+8A>T
NM_004360.4:c.2439+8A>T	NP_004351.1:n.2439+8A>T
NM_004360.5:c.2439+8A>T MANE Select	NP_004351.1:n.2439+8A>T
NM_001317184.2:c.2256+8A>T	NP_001304113.1:n.2256+8A>T
NM_001317185.2:c.891+8A>T	NP_001304114.1:n.891+8A>T
NM_001317186.2:c.474+8A>T	NP_001304115.1:n.474+8A>T