Canonical Allele Identifier: CA396464927
Gene: CDH1 HGNC NCBI

Linked Data

dbSNP Id: rs2152136790
MyVariant Identifiers: chr16:g.68853208A>T (hg19) chr16:g.68819305A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68819305A>T , CM000678.2:g.68819305A>T GRCh38
NC_000016.9:g.68853208A>T , CM000678.1:g.68853208A>T GRCh37
NC_000016.8:g.67410709A>T NCBI36
NG_008021.1:g.87014A>T , LRG_301:g.87014A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.1591A>T MANE Select ENSP00000261769.4:p.Asn531Tyr
ENST00000261769.9:c.1591A>T ENSP00000261769.4:p.Asn531Tyr
ENST00000422392.6:c.1408A>T ENSP00000414946.2:p.Asn470Tyr
ENST00000562836.5:n.1662A>T
ENST00000566510.5:c.*257A>T ENSP00000458139.1:n.*257A>T
ENST00000566612.5:c.1566-2696A>T ENSP00000454782.1:n.1566-2696A>T
ENST00000611625.4:c.1654A>T ENSP00000481063.1:p.Asn552Tyr
ENST00000612417.4:c.1591A>T ENSP00000478360.1:p.Asn531Tyr
ENST00000621016.4:c.1591A>T ENSP00000480664.1:p.Asn531Tyr
NM_004360.3:c.1591A>T , LRG_301t1:c.1591A>T NP_004351.1:p.Asn531Tyr
XM_011523488.1:c.856A>T XP_011521790.1:p.Asn286Tyr
XM_011523489.1:c.856A>T XP_011521791.1:p.Asn286Tyr
NM_001317184.1:c.1408A>T NP_001304113.1:p.Asn470Tyr
NM_001317185.1:c.43A>T NP_001304114.1:p.Asn15Tyr
NM_001317186.1:c.-254-2696A>T NP_001304115.1:n.-254-2696A>T
NM_004360.4:c.1591A>T NP_004351.1:p.Asn531Tyr
NM_004360.5:c.1591A>T MANE Select NP_004351.1:p.Asn531Tyr
NM_001317184.2:c.1408A>T NP_001304113.1:p.Asn470Tyr
NM_001317185.2:c.43A>T NP_001304114.1:p.Asn15Tyr
NM_001317186.2:c.-254-2696A>T NP_001304115.1:n.-254-2696A>T
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