Canonical Allele Identifier: CA2229916744
Gene: CDH1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68738402C= , CM000678.2:g.68738402C= GRCh38
NC_000016.9:g.68772305C= , CM000678.1:g.68772305C= GRCh37
NC_000016.8:g.67329806C= NCBI36
NG_008021.1:g.6111C= , LRG_301:g.6111C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.154C= MANE Select ENSP00000261769.4:p.Leu52=
ENST00000261769.9:c.154C= ENSP00000261769.4:p.Leu52=
ENST00000422392.6:c.154C= ENSP00000414946.2:p.Leu52=
ENST00000566510.5:c.154C= ENSP00000458139.1:p.Leu52=
ENST00000566612.5:c.154C= ENSP00000454782.1:p.Leu52=
ENST00000611625.4:c.154C= ENSP00000481063.1:p.Leu52=
ENST00000612417.4:c.154C= ENSP00000478360.1:p.Leu52=
ENST00000621016.4:c.154C= ENSP00000480664.1:p.Leu52=
NM_004360.3:c.154C= , LRG_301t1:c.154C= NP_004351.1:p.Leu52=
NM_001317184.1:c.154C= NP_001304113.1:p.Leu52=
NM_001317185.1:c.-1462C= NP_001304114.1:n.-1462C=
NM_001317186.1:c.-1666C= NP_001304115.1:n.-1666C=
NM_004360.4:c.154C= NP_004351.1:p.Leu52=
NM_004360.5:c.154C= MANE Select NP_004351.1:p.Leu52=
NM_001317184.2:c.154C= NP_001304113.1:p.Leu52=
NM_001317185.2:c.-1462C= NP_001304114.1:n.-1462C=
NM_001317186.2:c.-1666C= NP_001304115.1:n.-1666C=
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