Canonical Allele Identifier: CA2229983156

Gene: CDH1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68823537_68823539delinsCTG , CM000678.2:g.68823537_68823539delinsCTG	GRCh38
NC_000016.9:g.68857440_68857442delinsCTG , CM000678.1:g.68857440_68857442delinsCTG	GRCh37
NC_000016.8:g.67414941_67414943delinsCTG	NCBI36
NG_008021.1:g.91246_91248delinsCTG , LRG_301:g.91246_91248delinsCTG

Transcript Alleles

HGVS	Amino-acid change
ENST00000261769.10:c.2075_2077delinsCTG MANE Select	ENSP00000261769.4:p.Ala692=
ENST00000261769.9:c.2075_2077delinsCTG	ENSP00000261769.4:p.Ala692=
ENST00000422392.6:c.1892_1894delinsCTG	ENSP00000414946.2:p.Ala631=
ENST00000562118.1:n.293_295delinsCTG
ENST00000562836.5:n.2146_2148delinsCTG
ENST00000566510.5:c.*741_*743delinsCTG	ENSP00000458139.1:n.*741_*743delinsCTG
ENST00000566612.5:c.*315_*317delinsCTG	ENSP00000454782.1:n.*315_*317delinsCTG
ENST00000611625.4:c.2138_2140delinsCTG	ENSP00000481063.1:p.Ala713=
ENST00000612417.4:c.1830+1418_1830+1420delinsCTG	ENSP00000478360.1:n.1830+1418_1830+1420de...
ENST00000621016.4:c.1865+1383_1865+1385delinsCTG	ENSP00000480664.1:n.1865+1383_1865+1385de...
NM_004360.3:c.2075_2077delinsCTG , LRG_301t1:c.2075_2077delinsCTG	NP_004351.1:p.Ala692=
XM_011523488.1:c.1340_1342delinsCTG	XP_011521790.1:p.Ala447=
XM_011523489.1:c.1340_1342delinsCTG	XP_011521791.1:p.Ala447=
NM_001317184.1:c.1892_1894delinsCTG	NP_001304113.1:p.Ala631=
NM_001317185.1:c.527_529delinsCTG	NP_001304114.1:p.Ala176=
NM_001317186.1:c.110_112delinsCTG	NP_001304115.1:p.Ala37=
NM_004360.4:c.2075_2077delinsCTG	NP_004351.1:p.Ala692=
NM_004360.5:c.2075_2077delinsCTG MANE Select	NP_004351.1:p.Ala692=
NM_001317184.2:c.1892_1894delinsCTG	NP_001304113.1:p.Ala631=
NM_001317185.2:c.527_529delinsCTG	NP_001304114.1:p.Ala176=
NM_001317186.2:c.110_112delinsCTG	NP_001304115.1:p.Ala37=