Canonical Allele Identifier: CA2580092029

Gene: CDH1

Linked Data

• ClinVar Variation Id: 2035371
• ClinVar RCV Id: RCV002877481
• dbSNP Id: rs2152141614

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68828314G>C , CM000678.2:g.68828314G>C	GRCh38
NC_000016.9:g.68862217G>C , CM000678.1:g.68862217G>C	GRCh37
NC_000016.8:g.67419718G>C	NCBI36
NG_008021.1:g.96023G>C , LRG_301:g.96023G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000261769.10:c.2295+10G>C MANE Select	ENSP00000261769.4:n.2295+10G>C
ENST00000261769.9:c.2295+10G>C	ENSP00000261769.4:n.2295+10G>C
ENST00000422392.6:c.2112+10G>C	ENSP00000414946.2:n.2112+10G>C
ENST00000562118.1:n.513+10G>C
ENST00000562836.5:n.2366+10G>C
ENST00000566510.5:c.*961+10G>C	ENSP00000458139.1:n.*961+10G>C
ENST00000566612.5:c.*535+10G>C	ENSP00000454782.1:n.*535+10G>C
ENST00000611625.4:c.2358+10G>C	ENSP00000481063.1:n.2358+10G>C
ENST00000612417.4:c.1853+1760G>C	ENSP00000478360.1:n.1853+1760G>C
ENST00000621016.4:c.1866-5889G>C	ENSP00000480664.1:n.1866-5889G>C
NM_004360.3:c.2295+10G>C , LRG_301t1:c.2295+10G>C	NP_004351.1:n.2295+10G>C
XM_011523488.1:c.1560+10G>C	XP_011521790.1:n.1560+10G>C
XM_011523489.1:c.1560+10G>C	XP_011521791.1:n.1560+10G>C
NM_001317184.1:c.2112+10G>C	NP_001304113.1:n.2112+10G>C
NM_001317185.1:c.747+10G>C	NP_001304114.1:n.747+10G>C
NM_001317186.1:c.330+10G>C	NP_001304115.1:n.330+10G>C
NM_004360.4:c.2295+10G>C	NP_004351.1:n.2295+10G>C
NM_004360.5:c.2295+10G>C MANE Select	NP_004351.1:n.2295+10G>C
NM_001317184.2:c.2112+10G>C	NP_001304113.1:n.2112+10G>C
NM_001317185.2:c.747+10G>C	NP_001304114.1:n.747+10G>C
NM_001317186.2:c.330+10G>C	NP_001304115.1:n.330+10G>C