Canonical Allele Identifier: CA2229915201

Gene: CDH1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68737435_68737436delinsGC , CM000678.2:g.68737435_68737436delinsGC	GRCh38
NC_000016.9:g.68771338_68771339delinsGC , CM000678.1:g.68771338_68771339delinsGC	GRCh37
NC_000016.8:g.67328839_67328840delinsGC	NCBI36
NG_008021.1:g.5144_5145delinsGC , LRG_301:g.5144_5145delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261769.10:c.20_21delinsGC MANE Select	ENSP00000261769.4:p.Ser7=
ENST00000261769.9:c.20_21delinsGC	ENSP00000261769.4:p.Ser7=
ENST00000422392.6:c.20_21delinsGC	ENSP00000414946.2:p.Ser7=
ENST00000566510.5:c.20_21delinsGC	ENSP00000458139.1:p.Ser7=
ENST00000566612.5:c.20_21delinsGC	ENSP00000454782.1:p.Ser7=
ENST00000611625.4:c.20_21delinsGC	ENSP00000481063.1:p.Ser7=
ENST00000612417.4:c.20_21delinsGC	ENSP00000478360.1:p.Ser7=
ENST00000621016.4:c.20_21delinsGC	ENSP00000480664.1:p.Ser7=
NM_004360.3:c.20_21delinsGC , LRG_301t1:c.20_21delinsGC	NP_004351.1:p.Ser7=
NM_001317184.1:c.20_21delinsGC	NP_001304113.1:p.Ser7=
NM_001317185.1:c.-1596_-1595delinsGC	NP_001304114.1:n.-1596_-1595delinsGC
NM_001317186.1:c.-1800_-1799delinsGC	NP_001304115.1:n.-1800_-1799delinsGC
NM_004360.4:c.20_21delinsGC	NP_004351.1:p.Ser7=
NM_004360.5:c.20_21delinsGC MANE Select	NP_004351.1:p.Ser7=
NM_001317184.2:c.20_21delinsGC	NP_001304113.1:p.Ser7=
NM_001317185.2:c.-1596_-1595delinsGC	NP_001304114.1:n.-1596_-1595delinsGC
NM_001317186.2:c.-1800_-1799delinsGC	NP_001304115.1:n.-1800_-1799delinsGC