Canonical Allele Identifier: CA396470770

Gene: CDH1

Linked Data

• ClinVar Variation Id: 923471
• ClinVar RCV Id: RCV001184180
• dbSNP Id: rs1961424109
• MyVariant Identifiers: chr16:g.68863567T>C (hg19) ; chr16:g.68829664T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68829664T>C , CM000678.2:g.68829664T>C	GRCh38
NC_000016.9:g.68863567T>C , CM000678.1:g.68863567T>C	GRCh37
NC_000016.8:g.67421068T>C	NCBI36
NG_008021.1:g.97373T>C , LRG_301:g.97373T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000261769.10:c.2306T>C MANE Select	ENSP00000261769.4:p.Leu769Ser
ENST00000261769.9:c.2306T>C	ENSP00000261769.4:p.Leu769Ser
ENST00000422392.6:c.2123T>C	ENSP00000414946.2:p.Leu708Ser
ENST00000562118.1:n.524T>C
ENST00000562836.5:n.2377T>C
ENST00000566510.5:c.*972T>C	ENSP00000458139.1:n.*972T>C
ENST00000566612.5:c.*546T>C	ENSP00000454782.1:n.*546T>C
ENST00000611625.4:c.2369T>C	ENSP00000481063.1:p.Leu790Ser
ENST00000612417.4:c.1853+3110T>C	ENSP00000478360.1:n.1853+3110T>C
ENST00000621016.4:c.1866-4539T>C	ENSP00000480664.1:n.1866-4539T>C
NM_004360.3:c.2306T>C , LRG_301t1:c.2306T>C	NP_004351.1:p.Leu769Ser
XM_011523488.1:c.1571T>C	XP_011521790.1:p.Leu524Ser
XM_011523489.1:c.1571T>C	XP_011521791.1:p.Leu524Ser
NM_001317184.1:c.2123T>C	NP_001304113.1:p.Leu708Ser
NM_001317185.1:c.758T>C	NP_001304114.1:p.Leu253Ser
NM_001317186.1:c.341T>C	NP_001304115.1:p.Leu114Ser
NM_004360.4:c.2306T>C	NP_004351.1:p.Leu769Ser
NM_004360.5:c.2306T>C MANE Select	NP_004351.1:p.Leu769Ser
NM_001317184.2:c.2123T>C	NP_001304113.1:p.Leu708Ser
NM_001317185.2:c.758T>C	NP_001304114.1:p.Leu253Ser
NM_001317186.2:c.341T>C	NP_001304115.1:p.Leu114Ser