Canonical Allele Identifier: CA723137256
Gene: CDH1 HGNC NCBI

Linked Data

dbSNP Id: rs1356637268
gnomAD v3: 16-68819697-C-T
gnomAD v4: 16-68819697-C-T
MyVariant Identifiers: chr16:g.68853600C>T (hg19) chr16:g.68819697C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68819697C>T , CM000678.2:g.68819697C>T GRCh38
NC_000016.9:g.68853600C>T , CM000678.1:g.68853600C>T GRCh37
NC_000016.8:g.67411101C>T NCBI36
NG_008021.1:g.87406C>T , LRG_301:g.87406C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.1711+272C>T MANE Select ENSP00000261769.4:n.1711+272C>T
ENST00000261769.9:c.1711+272C>T ENSP00000261769.4:n.1711+272C>T
ENST00000422392.6:c.1528+272C>T ENSP00000414946.2:n.1528+272C>T
ENST00000562836.5:n.1782+272C>T
ENST00000566510.5:c.*377+272C>T ENSP00000458139.1:n.*377+272C>T
ENST00000566612.5:c.1566-2304C>T ENSP00000454782.1:n.1566-2304C>T
ENST00000611625.4:c.1774+272C>T ENSP00000481063.1:n.1774+272C>T
ENST00000612417.4:c.1711+272C>T ENSP00000478360.1:n.1711+272C>T
ENST00000621016.4:c.1711+272C>T ENSP00000480664.1:n.1711+272C>T
NM_004360.3:c.1711+272C>T , LRG_301t1:c.1711+272C>T NP_004351.1:n.1711+272C>T
XM_011523488.1:c.976+272C>T XP_011521790.1:n.976+272C>T
XM_011523489.1:c.976+272C>T XP_011521791.1:n.976+272C>T
NM_001317184.1:c.1528+272C>T NP_001304113.1:n.1528+272C>T
NM_001317185.1:c.163+272C>T NP_001304114.1:n.163+272C>T
NM_001317186.1:c.-254-2304C>T NP_001304115.1:n.-254-2304C>T
NM_004360.4:c.1711+272C>T NP_004351.1:n.1711+272C>T
NM_004360.5:c.1711+272C>T MANE Select NP_004351.1:n.1711+272C>T
NM_001317184.2:c.1528+272C>T NP_001304113.1:n.1528+272C>T
NM_001317185.2:c.163+272C>T NP_001304114.1:n.163+272C>T
NM_001317186.2:c.-254-2304C>T NP_001304115.1:n.-254-2304C>T
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