Canonical Allele Identifier: CA2229978284

Gene: CDH1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68833398_68833400delinsTCC , CM000678.2:g.68833398_68833400delinsTCC	GRCh38
NC_000016.9:g.68867301_68867303delinsTCC , CM000678.1:g.68867301_68867303delinsTCC	GRCh37
NC_000016.8:g.67424802_67424804delinsTCC	NCBI36
NG_008021.1:g.101107_101109delinsTCC , LRG_301:g.101107_101109delinsTCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261769.10:c.2548_2550delinsTCC MANE Select	ENSP00000261769.4:p.Ser850=
ENST00000261769.9:c.2548_2550delinsTCC	ENSP00000261769.4:p.Ser850=
ENST00000422392.6:c.2365_2367delinsTCC	ENSP00000414946.2:p.Ser789=
ENST00000562118.1:n.766_768delinsTCC
ENST00000562836.5:n.2619_2621delinsTCC
ENST00000566510.5:c.*1214_*1216delinsTCC	ENSP00000458139.1:n.*1214_*1216delinsTCC
ENST00000566612.5:c.*788_*790delinsTCC	ENSP00000454782.1:n.*788_*790delinsTCC
ENST00000611625.4:c.2611_2613delinsTCC	ENSP00000481063.1:p.Ser871=
ENST00000612417.4:c.1854-793_1854-791delinsTCC	ENSP00000478360.1:n.1854-793_1854-791delinsTCC
ENST00000621016.4:c.1866-805_1866-803delinsTCC	ENSP00000480664.1:n.1866-805_1866-803delinsTCC
NM_004360.3:c.2548_2550delinsTCC , LRG_301t1:c.2548_2550delinsTCC	NP_004351.1:p.Ser850=
XM_011523488.1:c.1813_1815delinsTCC	XP_011521790.1:p.Ser605=
XM_011523489.1:c.1813_1815delinsTCC	XP_011521791.1:p.Ser605=
NM_001317184.1:c.2365_2367delinsTCC	NP_001304113.1:p.Ser789=
NM_001317185.1:c.1000_1002delinsTCC	NP_001304114.1:p.Ser334=
NM_001317186.1:c.583_585delinsTCC	NP_001304115.1:p.Ser195=
NM_004360.4:c.2548_2550delinsTCC	NP_004351.1:p.Ser850=
NM_004360.5:c.2548_2550delinsTCC MANE Select	NP_004351.1:p.Ser850=
NM_001317184.2:c.2365_2367delinsTCC	NP_001304113.1:p.Ser789=
NM_001317185.2:c.1000_1002delinsTCC	NP_001304114.1:p.Ser334=
NM_001317186.2:c.583_585delinsTCC	NP_001304115.1:p.Ser195=