Canonical Allele Identifier: CA10580114

Gene: CDH1

Linked Data

• ClinVar Variation Id: 230755
• ClinVar RCV Id: RCV000213305 ; RCV000551088
• dbSNP Id: rs876658750
• gnomAD v4: 16-68815637-T-C
• MyVariant Identifiers: chr16:g.68849540T>C (hg19) ; chr16:g.68815637T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68815637T>C , CM000678.2:g.68815637T>C	GRCh38
NC_000016.9:g.68849540T>C , CM000678.1:g.68849540T>C	GRCh37
NC_000016.8:g.67407041T>C	NCBI36
NG_008021.1:g.83346T>C , LRG_301:g.83346T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261769.10:c.1443T>C MANE Select	ENSP00000261769.4:p.Asn481=
ENST00000261769.9:c.1443T>C	ENSP00000261769.4:p.Asn481=
ENST00000422392.6:c.1260T>C	ENSP00000414946.2:p.Asn420=
ENST00000562836.5:n.1514T>C
ENST00000566510.5:c.*109T>C	ENSP00000458139.1:n.*109T>C
ENST00000566612.5:c.1443T>C	ENSP00000454782.1:p.Asn481=
ENST00000611625.4:c.1506T>C	ENSP00000481063.1:p.Asn502=
ENST00000612417.4:c.1443T>C	ENSP00000478360.1:p.Asn481=
ENST00000621016.4:c.1443T>C	ENSP00000480664.1:p.Asn481=
NM_004360.3:c.1443T>C , LRG_301t1:c.1443T>C	NP_004351.1:p.Asn481=
XM_011523488.1:c.708T>C	XP_011521790.1:p.Asn236=
XM_011523489.1:c.708T>C	XP_011521791.1:p.Asn236=
NM_001317184.1:c.1260T>C	NP_001304113.1:p.Asn420=
NM_001317185.1:c.-106T>C	NP_001304114.1:n.-106T>C
NM_001317186.1:c.-377T>C	NP_001304115.1:n.-377T>C
NM_004360.4:c.1443T>C	NP_004351.1:p.Asn481=
NM_004360.5:c.1443T>C MANE Select	NP_004351.1:p.Asn481=
NM_001317184.2:c.1260T>C	NP_001304113.1:p.Asn420=
NM_001317185.2:c.-106T>C	NP_001304114.1:n.-106T>C
NM_001317186.2:c.-377T>C	NP_001304115.1:n.-377T>C