Canonical Allele Identifier: CA2229982712

Gene: CDH1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68823441_68823442delinsTG , CM000678.2:g.68823441_68823442delinsTG	GRCh38
NC_000016.9:g.68857344_68857345delinsTG , CM000678.1:g.68857344_68857345delinsTG	GRCh37
NC_000016.8:g.67414845_67414846delinsTG	NCBI36
NG_008021.1:g.91150_91151delinsTG , LRG_301:g.91150_91151delinsTG

Transcript Alleles

HGVS	Amino-acid change
ENST00000261769.10:c.1979_1980delinsTG MANE Select	ENSP00000261769.4:p.Val660=
ENST00000261769.9:c.1979_1980delinsTG	ENSP00000261769.4:p.Val660=
ENST00000422392.6:c.1796_1797delinsTG	ENSP00000414946.2:p.Val599=
ENST00000562118.1:n.197_198delinsTG
ENST00000562836.5:n.2050_2051delinsTG
ENST00000566510.5:c.*645_*646delinsTG	ENSP00000458139.1:n.*645_*646delinsTG
ENST00000566612.5:c.*219_*220delinsTG	ENSP00000454782.1:n.*219_*220delinsTG
ENST00000611625.4:c.2042_2043delinsTG	ENSP00000481063.1:p.Val681=
ENST00000612417.4:c.1830+1322_1830+1323delinsTG	ENSP00000478360.1:n.1830+1322_1830+1323de...
ENST00000621016.4:c.1865+1287_1865+1288delinsTG	ENSP00000480664.1:n.1865+1287_1865+1288de...
NM_004360.3:c.1979_1980delinsTG , LRG_301t1:c.1979_1980delinsTG	NP_004351.1:p.Val660=
XM_011523488.1:c.1244_1245delinsTG	XP_011521790.1:p.Val415=
XM_011523489.1:c.1244_1245delinsTG	XP_011521791.1:p.Val415=
NM_001317184.1:c.1796_1797delinsTG	NP_001304113.1:p.Val599=
NM_001317185.1:c.431_432delinsTG	NP_001304114.1:p.Val144=
NM_001317186.1:c.14_15delinsTG	NP_001304115.1:p.Val5=
NM_004360.4:c.1979_1980delinsTG	NP_004351.1:p.Val660=
NM_004360.5:c.1979_1980delinsTG MANE Select	NP_004351.1:p.Val660=
NM_001317184.2:c.1796_1797delinsTG	NP_001304113.1:p.Val599=
NM_001317185.2:c.431_432delinsTG	NP_001304114.1:p.Val144=
NM_001317186.2:c.14_15delinsTG	NP_001304115.1:p.Val5=