Canonical Allele Identifier: CA396458161

Gene: CDH1

Linked Data - Predicted Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68808849G>T , CM000678.2:g.68808849G>T	GRCh38
NC_000016.9:g.68842752G>T , CM000678.1:g.68842752G>T	GRCh37
NC_000016.8:g.67400253G>T	NCBI36
NG_008021.1:g.76558G>T , LRG_301:g.76558G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261769.10:c.687+1G>T MANE Select	ENSP00000261769.4:n.687+1G>T
ENST00000261769.9:c.687+1G>T	ENSP00000261769.4:n.687+1G>T
ENST00000422392.6:c.687+1G>T	ENSP00000414946.2:n.687+1G>T
ENST00000561751.1:c.454+1G>T
ENST00000562836.5:n.758+1G>T
ENST00000566510.5:c.531+282G>T	ENSP00000458139.1:n.531+282G>T
ENST00000566612.5:c.687+1G>T	ENSP00000454782.1:n.687+1G>T
ENST00000567320.1:n.198G>T
ENST00000611625.4:c.687+1G>T	ENSP00000481063.1:n.687+1G>T
ENST00000612417.4:c.687+1G>T	ENSP00000478360.1:n.687+1G>T
ENST00000621016.4:c.687+1G>T	ENSP00000480664.1:n.687+1G>T
NM_004360.3:c.687+1G>T , LRG_301t1:c.687+1G>T	NP_004351.1:n.687+1G>T
XM_011523488.1:c.-49+1G>T	XP_011521790.1:n.-49+1G>T
XM_011523489.1:c.-49+1G>T	XP_011521791.1:n.-49+1G>T
NM_001317184.1:c.687+1G>T	NP_001304113.1:n.687+1G>T
NM_001317185.1:c.-929+1G>T	NP_001304114.1:n.-929+1G>T
NM_001317186.1:c.-1133+1G>T	NP_001304115.1:n.-1133+1G>T
NM_004360.4:c.687+1G>T	NP_004351.1:n.687+1G>T
NM_004360.5:c.687+1G>T MANE Select	NP_004351.1:n.687+1G>T
NM_001317184.2:c.687+1G>T	NP_001304113.1:n.687+1G>T
NM_001317185.2:c.-929+1G>T	NP_001304114.1:n.-929+1G>T
NM_001317186.2:c.-1133+1G>T	NP_001304115.1:n.-1133+1G>T