Canonical Allele Identifier: CA396472350
Gene: CDH1 HGNC NCBI

Linked Data

dbSNP Id: rs2152144020
MyVariant Identifiers: chr16:g.68867290G>A (hg19) chr16:g.68833387G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68833387G>A , CM000678.2:g.68833387G>A GRCh38
NC_000016.9:g.68867290G>A , CM000678.1:g.68867290G>A GRCh37
NC_000016.8:g.67424791G>A NCBI36
NG_008021.1:g.101096G>A , LRG_301:g.101096G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.2537G>A MANE Select ENSP00000261769.4:p.Ser846Asn
ENST00000261769.9:c.2537G>A ENSP00000261769.4:p.Ser846Asn
ENST00000422392.6:c.2354G>A ENSP00000414946.2:p.Ser785Asn
ENST00000562118.1:n.755G>A
ENST00000562836.5:n.2608G>A
ENST00000566510.5:c.*1203G>A ENSP00000458139.1:n.*1203G>A
ENST00000566612.5:c.*777G>A ENSP00000454782.1:n.*777G>A
ENST00000611625.4:c.2600G>A ENSP00000481063.1:p.Ser867Asn
ENST00000612417.4:c.1854-804G>A ENSP00000478360.1:n.1854-804G>A
ENST00000621016.4:c.1866-816G>A ENSP00000480664.1:n.1866-816G>A
NM_004360.3:c.2537G>A , LRG_301t1:c.2537G>A NP_004351.1:p.Ser846Asn
XM_011523488.1:c.1802G>A XP_011521790.1:p.Ser601Asn
XM_011523489.1:c.1802G>A XP_011521791.1:p.Ser601Asn
NM_001317184.1:c.2354G>A NP_001304113.1:p.Ser785Asn
NM_001317185.1:c.989G>A NP_001304114.1:p.Ser330Asn
NM_001317186.1:c.572G>A NP_001304115.1:p.Ser191Asn
NM_004360.4:c.2537G>A NP_004351.1:p.Ser846Asn
NM_004360.5:c.2537G>A MANE Select NP_004351.1:p.Ser846Asn
NM_001317184.2:c.2354G>A NP_001304113.1:p.Ser785Asn
NM_001317185.2:c.989G>A NP_001304114.1:p.Ser330Asn
NM_001317186.2:c.572G>A NP_001304115.1:p.Ser191Asn
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