Canonical Allele Identifier: CA2229980642
Gene: CDH1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68822127_68822130delinsACAT , CM000678.2:g.68822127_68822130delinsACAT GRCh38
NC_000016.9:g.68856030_68856033delinsACAT , CM000678.1:g.68856030_68856033delinsACAT GRCh37
NC_000016.8:g.67413531_67413534delinsACAT NCBI36
NG_008021.1:g.89836_89839delinsACAT , LRG_301:g.89836_89839delinsACAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.1838_1841delinsACAT MANE Select ENSP00000261769.4:p.Asn613=
ENST00000261769.9:c.1838_1841delinsACAT ENSP00000261769.4:p.Asn613=
ENST00000422392.6:c.1655_1658delinsACAT ENSP00000414946.2:p.Asn552=
ENST00000562836.5:n.1909_1912delinsACAT
ENST00000566510.5:c.*504_*507delinsACAT ENSP00000458139.1:n.*504_*507delinsACAT
ENST00000566612.5:c.*78_*81delinsACAT ENSP00000454782.1:n.*78_*81delinsACAT
ENST00000611625.4:c.1901_1904delinsACAT ENSP00000481063.1:p.Asn634=
ENST00000612417.4:c.1830+8_1830+11delinsACAT ENSP00000478360.1:n.1830+8_1830+11delinsACAT
ENST00000621016.4:c.1838_1841delinsACAT ENSP00000480664.1:p.Asn613=
NM_004360.3:c.1838_1841delinsACAT , LRG_301t1:c.1838_1841delinsACAT NP_004351.1:p.Asn613=
XM_011523488.1:c.1103_1106delinsACAT XP_011521790.1:p.Asn368=
XM_011523489.1:c.1103_1106delinsACAT XP_011521791.1:p.Asn368=
NM_001317184.1:c.1655_1658delinsACAT NP_001304113.1:p.Asn552=
NM_001317185.1:c.290_293delinsACAT NP_001304114.1:p.Asn97=
NM_001317186.1:c.-128_-125delinsACAT NP_001304115.1:n.-128_-125delinsACAT
NM_004360.4:c.1838_1841delinsACAT NP_004351.1:p.Asn613=
NM_004360.5:c.1838_1841delinsACAT MANE Select NP_004351.1:p.Asn613=
NM_001317184.2:c.1655_1658delinsACAT NP_001304113.1:p.Asn552=
NM_001317185.2:c.290_293delinsACAT NP_001304114.1:p.Asn97=
NM_001317186.2:c.-128_-125delinsACAT NP_001304115.1:n.-128_-125delinsACAT