Canonical Allele Identifier: CA396467645

Gene: CDH1

Linked Data

• dbSNP Id: rs2152139367
• MyVariant Identifiers: chr16:g.68857369G>C (hg19) ; chr16:g.68823466G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68823466G>C , CM000678.2:g.68823466G>C	GRCh38
NC_000016.9:g.68857369G>C , CM000678.1:g.68857369G>C	GRCh37
NC_000016.8:g.67414870G>C	NCBI36
NG_008021.1:g.91175G>C , LRG_301:g.91175G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000261769.10:c.2004G>C MANE Select	ENSP00000261769.4:p.Lys668Asn
ENST00000261769.9:c.2004G>C	ENSP00000261769.4:p.Lys668Asn
ENST00000422392.6:c.1821G>C	ENSP00000414946.2:p.Lys607Asn
ENST00000562118.1:n.222G>C
ENST00000562836.5:n.2075G>C
ENST00000566510.5:c.*670G>C	ENSP00000458139.1:n.*670G>C
ENST00000566612.5:c.*244G>C	ENSP00000454782.1:n.*244G>C
ENST00000611625.4:c.2067G>C	ENSP00000481063.1:p.Lys689Asn
ENST00000612417.4:c.1830+1347G>C	ENSP00000478360.1:n.1830+1347G>C
ENST00000621016.4:c.1865+1312G>C	ENSP00000480664.1:n.1865+1312G>C
NM_004360.3:c.2004G>C , LRG_301t1:c.2004G>C	NP_004351.1:p.Lys668Asn
XM_011523488.1:c.1269G>C	XP_011521790.1:p.Lys423Asn
XM_011523489.1:c.1269G>C	XP_011521791.1:p.Lys423Asn
NM_001317184.1:c.1821G>C	NP_001304113.1:p.Lys607Asn
NM_001317185.1:c.456G>C	NP_001304114.1:p.Lys152Asn
NM_001317186.1:c.39G>C	NP_001304115.1:p.Lys13Asn
NM_004360.4:c.2004G>C	NP_004351.1:p.Lys668Asn
NM_004360.5:c.2004G>C MANE Select	NP_004351.1:p.Lys668Asn
NM_001317184.2:c.1821G>C	NP_001304113.1:p.Lys607Asn
NM_001317185.2:c.456G>C	NP_001304114.1:p.Lys152Asn
NM_001317186.2:c.39G>C	NP_001304115.1:p.Lys13Asn