Canonical Allele Identifier: CA396471176
Gene: CDH1 HGNC NCBI

Linked Data

gnomAD v4: 16-68829749-T-A
MyVariant Identifiers: chr16:g.68863652T>A (hg19) chr16:g.68829749T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68829749T>A , CM000678.2:g.68829749T>A GRCh38
NC_000016.9:g.68863652T>A , CM000678.1:g.68863652T>A GRCh37
NC_000016.8:g.67421153T>A NCBI36
NG_008021.1:g.97458T>A , LRG_301:g.97458T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.2391T>A MANE Select ENSP00000261769.4:p.Tyr797Ter
ENST00000261769.9:c.2391T>A ENSP00000261769.4:p.Tyr797Ter
ENST00000422392.6:c.2208T>A ENSP00000414946.2:p.Tyr736Ter
ENST00000562118.1:n.609T>A
ENST00000562836.5:n.2462T>A
ENST00000566510.5:c.*1057T>A ENSP00000458139.1:n.*1057T>A
ENST00000566612.5:c.*631T>A ENSP00000454782.1:n.*631T>A
ENST00000611625.4:c.2454T>A ENSP00000481063.1:p.Tyr818Ter
ENST00000612417.4:c.1853+3195T>A ENSP00000478360.1:n.1853+3195T>A
ENST00000621016.4:c.1866-4454T>A ENSP00000480664.1:n.1866-4454T>A
NM_004360.3:c.2391T>A , LRG_301t1:c.2391T>A NP_004351.1:p.Tyr797Ter
XM_011523488.1:c.1656T>A XP_011521790.1:p.Tyr552Ter
XM_011523489.1:c.1656T>A XP_011521791.1:p.Tyr552Ter
NM_001317184.1:c.2208T>A NP_001304113.1:p.Tyr736Ter
NM_001317185.1:c.843T>A NP_001304114.1:p.Tyr281Ter
NM_001317186.1:c.426T>A NP_001304115.1:p.Tyr142Ter
NM_004360.4:c.2391T>A NP_004351.1:p.Tyr797Ter
NM_004360.5:c.2391T>A MANE Select NP_004351.1:p.Tyr797Ter
NM_001317184.2:c.2208T>A NP_001304113.1:p.Tyr736Ter
NM_001317185.2:c.843T>A NP_001304114.1:p.Tyr281Ter
NM_001317186.2:c.426T>A NP_001304115.1:p.Tyr142Ter
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