Canonical Allele Identifier: CA623136693
Gene: CDH1 HGNC NCBI

Linked Data

dbSNP Id: rs1250672623
gnomAD v2: 16-68844309-T-G
gnomAD v3: 16-68810406-T-G
gnomAD v4: 16-68810406-T-G
MyVariant Identifiers: chr16:g.68844309T>G (hg19) chr16:g.68810406T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68810406T>G , CM000678.2:g.68810406T>G GRCh38
NC_000016.9:g.68844309T>G , CM000678.1:g.68844309T>G GRCh37
NC_000016.8:g.67401810T>G NCBI36
NG_008021.1:g.78115T>G , LRG_301:g.78115T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.832+65T>G MANE Select ENSP00000261769.4:n.832+65T>G
ENST00000261769.9:c.832+65T>G ENSP00000261769.4:n.832+65T>G
ENST00000422392.6:c.832+65T>G ENSP00000414946.2:n.832+65T>G
ENST00000561751.1:c.455-1278T>G
ENST00000562836.5:n.903+65T>G
ENST00000566510.5:c.676+65T>G ENSP00000458139.1:n.676+65T>G
ENST00000566612.5:c.832+65T>G ENSP00000454782.1:n.832+65T>G
ENST00000611625.4:c.832+65T>G ENSP00000481063.1:n.832+65T>G
ENST00000612417.4:c.832+65T>G ENSP00000478360.1:n.832+65T>G
ENST00000621016.4:c.832+65T>G ENSP00000480664.1:n.832+65T>G
NM_004360.3:c.832+65T>G , LRG_301t1:c.832+65T>G NP_004351.1:n.832+65T>G
XM_011523488.1:c.97+65T>G XP_011521790.1:n.97+65T>G
XM_011523489.1:c.97+65T>G XP_011521791.1:n.97+65T>G
NM_001317184.1:c.832+65T>G NP_001304113.1:n.832+65T>G
NM_001317185.1:c.-784+65T>G NP_001304114.1:n.-784+65T>G
NM_001317186.1:c.-988+65T>G NP_001304115.1:n.-988+65T>G
NM_004360.4:c.832+65T>G NP_004351.1:n.832+65T>G
NM_004360.5:c.832+65T>G MANE Select NP_004351.1:n.832+65T>G
NM_001317184.2:c.832+65T>G NP_001304113.1:n.832+65T>G
NM_001317185.2:c.-784+65T>G NP_001304114.1:n.-784+65T>G
NM_001317186.2:c.-988+65T>G NP_001304115.1:n.-988+65T>G
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