Canonical Allele Identifier: CA396470835
Gene: CDH1 HGNC NCBI

Linked Data

dbSNP Id: rs1961424604
MyVariant Identifiers: chr16:g.68863575C>G (hg19) chr16:g.68829672C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68829672C>G , CM000678.2:g.68829672C>G GRCh38
NC_000016.9:g.68863575C>G , CM000678.1:g.68863575C>G GRCh37
NC_000016.8:g.67421076C>G NCBI36
NG_008021.1:g.97381C>G , LRG_301:g.97381C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.2314C>G MANE Select ENSP00000261769.4:p.Leu772Val
ENST00000261769.9:c.2314C>G ENSP00000261769.4:p.Leu772Val
ENST00000422392.6:c.2131C>G ENSP00000414946.2:p.Leu711Val
ENST00000562118.1:n.532C>G
ENST00000562836.5:n.2385C>G
ENST00000566510.5:c.*980C>G ENSP00000458139.1:n.*980C>G
ENST00000566612.5:c.*554C>G ENSP00000454782.1:n.*554C>G
ENST00000611625.4:c.2377C>G ENSP00000481063.1:p.Leu793Val
ENST00000612417.4:c.1853+3118C>G ENSP00000478360.1:n.1853+3118C>G
ENST00000621016.4:c.1866-4531C>G ENSP00000480664.1:n.1866-4531C>G
NM_004360.3:c.2314C>G , LRG_301t1:c.2314C>G NP_004351.1:p.Leu772Val
XM_011523488.1:c.1579C>G XP_011521790.1:p.Leu527Val
XM_011523489.1:c.1579C>G XP_011521791.1:p.Leu527Val
NM_001317184.1:c.2131C>G NP_001304113.1:p.Leu711Val
NM_001317185.1:c.766C>G NP_001304114.1:p.Leu256Val
NM_001317186.1:c.349C>G NP_001304115.1:p.Leu117Val
NM_004360.4:c.2314C>G NP_004351.1:p.Leu772Val
NM_004360.5:c.2314C>G MANE Select NP_004351.1:p.Leu772Val
NM_001317184.2:c.2131C>G NP_001304113.1:p.Leu711Val
NM_001317185.2:c.766C>G NP_001304114.1:p.Leu256Val
NM_001317186.2:c.349C>G NP_001304115.1:p.Leu117Val
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