Canonical Allele Identifier: CA496393047
Gene: CDH1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr16:g.68867231T>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68833328T>G , CM000678.2:g.68833328T>G GRCh38
NC_000016.9:g.68867231T>G , CM000678.1:g.68867231T>G GRCh37
NC_000016.8:g.67424732T>G NCBI36
NG_008021.1:g.101037T>G , LRG_301:g.101037T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.2478T>G MANE Select ENSP00000261769.4:p.Pro826=
ENST00000261769.9:c.2478T>G ENSP00000261769.4:p.Pro826=
ENST00000422392.6:c.2295T>G ENSP00000414946.2:p.Pro765=
ENST00000562118.1:n.696T>G
ENST00000562836.5:n.2549T>G
ENST00000566510.5:c.*1144T>G ENSP00000458139.1:n.*1144T>G
ENST00000566612.5:c.*718T>G ENSP00000454782.1:n.*718T>G
ENST00000611625.4:c.2541T>G ENSP00000481063.1:p.Pro847=
ENST00000612417.4:c.1854-863T>G ENSP00000478360.1:n.1854-863T>G
ENST00000621016.4:c.1866-875T>G ENSP00000480664.1:n.1866-875T>G
NM_004360.3:c.2478T>G , LRG_301t1:c.2478T>G NP_004351.1:p.Pro826=
XM_011523488.1:c.1743T>G XP_011521790.1:p.Pro581=
XM_011523489.1:c.1743T>G XP_011521791.1:p.Pro581=
NM_001317184.1:c.2295T>G NP_001304113.1:p.Pro765=
NM_001317185.1:c.930T>G NP_001304114.1:p.Pro310=
NM_001317186.1:c.513T>G NP_001304115.1:p.Pro171=
NM_004360.4:c.2478T>G NP_004351.1:p.Pro826=
NM_004360.5:c.2478T>G MANE Select NP_004351.1:p.Pro826=
NM_001317184.2:c.2295T>G NP_001304113.1:p.Pro765=
NM_001317185.2:c.930T>G NP_001304114.1:p.Pro310=
NM_001317186.2:c.513T>G NP_001304115.1:p.Pro171=
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