Canonical Allele Identifier: CA283319497
Gene: CDH1 HGNC NCBI

Linked Data

dbSNP Id: rs1003174610
gnomAD v2: 16-68866724-T-TA
gnomAD v3: 16-68832821-T-TA
gnomAD v4: 16-68832821-T-TA
MyVariant Identifiers: chr16:g.68866724_68866725insA (hg19) chr16:g.68832821_68832822insA (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68832830dup , CM000678.2:g.68832830dup GRCh38
NC_000016.9:g.68866733dup , CM000678.1:g.68866733dup GRCh37
NC_000016.8:g.67424234dup NCBI36
NG_008021.1:g.100539dup , LRG_301:g.100539dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.2440-460dup MANE Select ENSP00000261769.4:n.2440-460dup
ENST00000261769.9:c.2440-460dup ENSP00000261769.4:n.2440-460dup
ENST00000422392.6:c.2257-460dup ENSP00000414946.2:n.2257-460dup
ENST00000562118.1:n.658-460dup
ENST00000562836.5:n.2511-460dup
ENST00000566510.5:c.*1106-460dup ENSP00000458139.1:n.*1106-460dup
ENST00000566612.5:c.*680-460dup ENSP00000454782.1:n.*680-460dup
ENST00000611625.4:c.2503-460dup ENSP00000481063.1:n.2503-460dup
ENST00000612417.4:c.1854-1361dup ENSP00000478360.1:n.1854-1361dup
ENST00000621016.4:c.1866-1373dup ENSP00000480664.1:n.1866-1373dup
NM_004360.3:c.2440-460dup , LRG_301t1:c.2440-460dup NP_004351.1:n.2440-460dup
XM_011523488.1:c.1705-460dup XP_011521790.1:n.1705-460dup
XM_011523489.1:c.1705-460dup XP_011521791.1:n.1705-460dup
NM_001317184.1:c.2257-460dup NP_001304113.1:n.2257-460dup
NM_001317185.1:c.892-460dup NP_001304114.1:n.892-460dup
NM_001317186.1:c.475-460dup NP_001304115.1:n.475-460dup
NM_004360.4:c.2440-460dup NP_004351.1:n.2440-460dup
NM_004360.5:c.2440-460dup MANE Select NP_004351.1:n.2440-460dup
NM_001317184.2:c.2257-460dup NP_001304113.1:n.2257-460dup
NM_001317185.2:c.892-460dup NP_001304114.1:n.892-460dup
NM_001317186.2:c.475-460dup NP_001304115.1:n.475-460dup
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