Canonical Allele Identifier: CA396471165
Gene: CDH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2494013
ClinVar RCV Id: RCV003206438
MyVariant Identifiers: chr16:g.68863650T>G (hg19) chr16:g.68829747T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68829747T>G , CM000678.2:g.68829747T>G GRCh38
NC_000016.9:g.68863650T>G , CM000678.1:g.68863650T>G GRCh37
NC_000016.8:g.67421151T>G NCBI36
NG_008021.1:g.97456T>G , LRG_301:g.97456T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.2389T>G MANE Select ENSP00000261769.4:p.Tyr797Asp
ENST00000261769.9:c.2389T>G ENSP00000261769.4:p.Tyr797Asp
ENST00000422392.6:c.2206T>G ENSP00000414946.2:p.Tyr736Asp
ENST00000562118.1:n.607T>G
ENST00000562836.5:n.2460T>G
ENST00000566510.5:c.*1055T>G ENSP00000458139.1:n.*1055T>G
ENST00000566612.5:c.*629T>G ENSP00000454782.1:n.*629T>G
ENST00000611625.4:c.2452T>G ENSP00000481063.1:p.Tyr818Asp
ENST00000612417.4:c.1853+3193T>G ENSP00000478360.1:n.1853+3193T>G
ENST00000621016.4:c.1866-4456T>G ENSP00000480664.1:n.1866-4456T>G
NM_004360.3:c.2389T>G , LRG_301t1:c.2389T>G NP_004351.1:p.Tyr797Asp
XM_011523488.1:c.1654T>G XP_011521790.1:p.Tyr552Asp
XM_011523489.1:c.1654T>G XP_011521791.1:p.Tyr552Asp
NM_001317184.1:c.2206T>G NP_001304113.1:p.Tyr736Asp
NM_001317185.1:c.841T>G NP_001304114.1:p.Tyr281Asp
NM_001317186.1:c.424T>G NP_001304115.1:p.Tyr142Asp
NM_004360.4:c.2389T>G NP_004351.1:p.Tyr797Asp
NM_004360.5:c.2389T>G MANE Select NP_004351.1:p.Tyr797Asp
NM_001317184.2:c.2206T>G NP_001304113.1:p.Tyr736Asp
NM_001317185.2:c.841T>G NP_001304114.1:p.Tyr281Asp
NM_001317186.2:c.424T>G NP_001304115.1:p.Tyr142Asp
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