Canonical Allele Identifier: CA2229983179

Gene: CDH1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68823540_68823547delinsGCGTCTGT , CM000678.2:g.68823540_68823547delinsGCGTCTGT	GRCh38
NC_000016.9:g.68857443_68857450delinsGCGTCTGT , CM000678.1:g.68857443_68857450delinsGCGTCTGT	GRCh37
NC_000016.8:g.67414944_67414951delinsGCGTCTGT	NCBI36
NG_008021.1:g.91249_91256delinsGCGTCTGT , LRG_301:g.91249_91256delinsGCGTCTGT

Transcript Alleles

HGVS	Amino-acid change
ENST00000261769.10:c.2078_2085delinsGCGTCTGT MANE Select	ENSP00000261769.4:p.Gly693=
ENST00000261769.9:c.2078_2085delinsGCGTCTGT	ENSP00000261769.4:p.Gly693=
ENST00000422392.6:c.1895_1902delinsGCGTCTGT	ENSP00000414946.2:p.Gly632=
ENST00000562118.1:n.296_303delinsGCGTCTGT
ENST00000562836.5:n.2149_2156delinsGCGTCTGT
ENST00000566510.5:c.*744_*751delinsGCGTCTGT	ENSP00000458139.1:n.*744_*751delinsGCGTCT...
ENST00000566612.5:c.*318_*325delinsGCGTCTGT	ENSP00000454782.1:n.*318_*325delinsGCGTCT...
ENST00000611625.4:c.2141_2148delinsGCGTCTGT	ENSP00000481063.1:p.Gly714=
ENST00000612417.4:c.1830+1421_1830+1428delinsGCGTCTGT	ENSP00000478360.1:n.1830+1421_1830+1428de...
ENST00000621016.4:c.1865+1386_1865+1393delinsGCGTCTGT	ENSP00000480664.1:n.1865+1386_1865+1393de...
NM_004360.3:c.2078_2085delinsGCGTCTGT , LRG_301t1:c.2078_2085delinsGCGTCTGT	NP_004351.1:p.Gly693=
XM_011523488.1:c.1343_1350delinsGCGTCTGT	XP_011521790.1:p.Gly448=
XM_011523489.1:c.1343_1350delinsGCGTCTGT	XP_011521791.1:p.Gly448=
NM_001317184.1:c.1895_1902delinsGCGTCTGT	NP_001304113.1:p.Gly632=
NM_001317185.1:c.530_537delinsGCGTCTGT	NP_001304114.1:p.Gly177=
NM_001317186.1:c.113_120delinsGCGTCTGT	NP_001304115.1:p.Gly38=
NM_004360.4:c.2078_2085delinsGCGTCTGT	NP_004351.1:p.Gly693=
NM_004360.5:c.2078_2085delinsGCGTCTGT MANE Select	NP_004351.1:p.Gly693=
NM_001317184.2:c.1895_1902delinsGCGTCTGT	NP_001304113.1:p.Gly632=
NM_001317185.2:c.530_537delinsGCGTCTGT	NP_001304114.1:p.Gly177=
NM_001317186.2:c.113_120delinsGCGTCTGT	NP_001304115.1:p.Gly38=