Canonical Allele Identifier: CA913188709
Gene: CDH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 923416
ClinVar RCV Id: RCV001184116
dbSNP Id: rs1962424166

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68737435_68737436delinsAT , CM000678.2:g.68737435_68737436delinsAT GRCh38
NC_000016.9:g.68771338_68771339delinsAT , CM000678.1:g.68771338_68771339delinsAT GRCh37
NC_000016.8:g.67328839_67328840delinsAT NCBI36
NG_008021.1:g.5144_5145delinsAT , LRG_301:g.5144_5145delinsAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.20_21delinsAT MANE Select ENSP00000261769.4:p.Ser7Asn
ENST00000261769.9:c.20_21delinsAT ENSP00000261769.4:p.Ser7Asn
ENST00000422392.6:c.20_21delinsAT ENSP00000414946.2:p.Ser7Asn
ENST00000566510.5:c.20_21delinsAT ENSP00000458139.1:p.Ser7Asn
ENST00000566612.5:c.20_21delinsAT ENSP00000454782.1:p.Ser7Asn
ENST00000611625.4:c.20_21delinsAT ENSP00000481063.1:p.Ser7Asn
ENST00000612417.4:c.20_21delinsAT ENSP00000478360.1:p.Ser7Asn
ENST00000621016.4:c.20_21delinsAT ENSP00000480664.1:p.Ser7Asn
NM_004360.3:c.20_21delinsAT , LRG_301t1:c.20_21delinsAT NP_004351.1:p.Ser7Asn
NM_001317184.1:c.20_21delinsAT NP_001304113.1:p.Ser7Asn
NM_001317185.1:c.-1596_-1595delinsAT NP_001304114.1:n.-1596_-1595delinsAT
NM_001317186.1:c.-1800_-1799delinsAT NP_001304115.1:n.-1800_-1799delinsAT
NM_004360.4:c.20_21delinsAT NP_004351.1:p.Ser7Asn
NM_004360.5:c.20_21delinsAT MANE Select NP_004351.1:p.Ser7Asn
NM_001317184.2:c.20_21delinsAT NP_001304113.1:p.Ser7Asn
NM_001317185.2:c.-1596_-1595delinsAT NP_001304114.1:n.-1596_-1595delinsAT
NM_001317186.2:c.-1800_-1799delinsAT NP_001304115.1:n.-1800_-1799delinsAT