Canonical Allele Identifier: CA496393060

Gene: CDH1

Linked Data

• ClinVar Variation Id: 532491
• ClinVar RCV Id: RCV000639308
• dbSNP Id: rs1555518229
• MyVariant Identifiers: chr16:g.68867240T>C (hg19) ; chr16:g.68833337T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68833337T>C , CM000678.2:g.68833337T>C	GRCh38
NC_000016.9:g.68867240T>C , CM000678.1:g.68867240T>C	GRCh37
NC_000016.8:g.67424741T>C	NCBI36
NG_008021.1:g.101046T>C , LRG_301:g.101046T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261769.10:c.2487T>C MANE Select	ENSP00000261769.4:p.Ser829=
ENST00000261769.9:c.2487T>C	ENSP00000261769.4:p.Ser829=
ENST00000422392.6:c.2304T>C	ENSP00000414946.2:p.Ser768=
ENST00000562118.1:n.705T>C
ENST00000562836.5:n.2558T>C
ENST00000566510.5:c.*1153T>C	ENSP00000458139.1:n.*1153T>C
ENST00000566612.5:c.*727T>C	ENSP00000454782.1:n.*727T>C
ENST00000611625.4:c.2550T>C	ENSP00000481063.1:p.Ser850=
ENST00000612417.4:c.1854-854T>C	ENSP00000478360.1:n.1854-854T>C
ENST00000621016.4:c.1866-866T>C	ENSP00000480664.1:n.1866-866T>C
NM_004360.3:c.2487T>C , LRG_301t1:c.2487T>C	NP_004351.1:p.Ser829=
XM_011523488.1:c.1752T>C	XP_011521790.1:p.Ser584=
XM_011523489.1:c.1752T>C	XP_011521791.1:p.Ser584=
NM_001317184.1:c.2304T>C	NP_001304113.1:p.Ser768=
NM_001317185.1:c.939T>C	NP_001304114.1:p.Ser313=
NM_001317186.1:c.522T>C	NP_001304115.1:p.Ser174=
NM_004360.4:c.2487T>C	NP_004351.1:p.Ser829=
NM_004360.5:c.2487T>C MANE Select	NP_004351.1:p.Ser829=
NM_001317184.2:c.2304T>C	NP_001304113.1:p.Ser768=
NM_001317185.2:c.939T>C	NP_001304114.1:p.Ser313=
NM_001317186.2:c.522T>C	NP_001304115.1:p.Ser174=