Canonical Allele Identifier: CA496157457
Gene: CDH1 HGNC NCBI

Linked Data

dbSNP Id: rs1411069226
MyVariant Identifiers: chr16:g.68863634C>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68829731C>G , CM000678.2:g.68829731C>G GRCh38
NC_000016.9:g.68863634C>G , CM000678.1:g.68863634C>G GRCh37
NC_000016.8:g.67421135C>G NCBI36
NG_008021.1:g.97440C>G , LRG_301:g.97440C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.2373C>G MANE Select ENSP00000261769.4:p.Leu791=
ENST00000261769.9:c.2373C>G ENSP00000261769.4:p.Leu791=
ENST00000422392.6:c.2190C>G ENSP00000414946.2:p.Leu730=
ENST00000562118.1:n.591C>G
ENST00000562836.5:n.2444C>G
ENST00000566510.5:c.*1039C>G ENSP00000458139.1:n.*1039C>G
ENST00000566612.5:c.*613C>G ENSP00000454782.1:n.*613C>G
ENST00000611625.4:c.2436C>G ENSP00000481063.1:p.Leu812=
ENST00000612417.4:c.1853+3177C>G ENSP00000478360.1:n.1853+3177C>G
ENST00000621016.4:c.1866-4472C>G ENSP00000480664.1:n.1866-4472C>G
NM_004360.3:c.2373C>G , LRG_301t1:c.2373C>G NP_004351.1:p.Leu791=
XM_011523488.1:c.1638C>G XP_011521790.1:p.Leu546=
XM_011523489.1:c.1638C>G XP_011521791.1:p.Leu546=
NM_001317184.1:c.2190C>G NP_001304113.1:p.Leu730=
NM_001317185.1:c.825C>G NP_001304114.1:p.Leu275=
NM_001317186.1:c.408C>G NP_001304115.1:p.Leu136=
NM_004360.4:c.2373C>G NP_004351.1:p.Leu791=
NM_004360.5:c.2373C>G MANE Select NP_004351.1:p.Leu791=
NM_001317184.2:c.2190C>G NP_001304113.1:p.Leu730=
NM_001317185.2:c.825C>G NP_001304114.1:p.Leu275=
NM_001317186.2:c.408C>G NP_001304115.1:p.Leu136=
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