Canonical Allele Identifier: CA396459006
Gene: CDH1 HGNC NCBI

Linked Data

dbSNP Id: rs864622346
MyVariant Identifiers: chr16:g.68844241C>G (hg19) chr16:g.68810338C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68810338C>G , CM000678.2:g.68810338C>G GRCh38
NC_000016.9:g.68844241C>G , CM000678.1:g.68844241C>G GRCh37
NC_000016.8:g.67401742C>G NCBI36
NG_008021.1:g.78047C>G , LRG_301:g.78047C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.829C>G MANE Select ENSP00000261769.4:p.Pro277Ala
ENST00000261769.9:c.829C>G ENSP00000261769.4:p.Pro277Ala
ENST00000422392.6:c.829C>G ENSP00000414946.2:p.Pro277Ala
ENST00000561751.1:c.455-1346C>G
ENST00000562836.5:n.900C>G
ENST00000566510.5:c.673C>G ENSP00000458139.1:p.Pro225Ala
ENST00000566612.5:c.829C>G ENSP00000454782.1:p.Pro277Ala
ENST00000611625.4:c.829C>G ENSP00000481063.1:p.Pro277Ala
ENST00000612417.4:c.829C>G ENSP00000478360.1:p.Pro277Ala
ENST00000621016.4:c.829C>G ENSP00000480664.1:p.Pro277Ala
NM_004360.3:c.829C>G , LRG_301t1:c.829C>G NP_004351.1:p.Pro277Ala
XM_011523488.1:c.94C>G XP_011521790.1:p.Pro32Ala
XM_011523489.1:c.94C>G XP_011521791.1:p.Pro32Ala
NM_001317184.1:c.829C>G NP_001304113.1:p.Pro277Ala
NM_001317185.1:c.-787C>G NP_001304114.1:n.-787C>G
NM_001317186.1:c.-991C>G NP_001304115.1:n.-991C>G
NM_004360.4:c.829C>G NP_004351.1:p.Pro277Ala
NM_004360.5:c.829C>G MANE Select NP_004351.1:p.Pro277Ala
NM_001317184.2:c.829C>G NP_001304113.1:p.Pro277Ala
NM_001317185.2:c.-787C>G NP_001304114.1:n.-787C>G
NM_001317186.2:c.-991C>G NP_001304115.1:n.-991C>G
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