Canonical Allele Identifier: CA396451427

Gene: CDH1

Linked Data

• ClinVar Variation Id: 1040346
• ClinVar RCV Id: RCV001343962
• dbSNP Id: rs749591910
• MyVariant Identifiers: chr16:g.68771366G>C (hg19) ; chr16:g.68737463G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68737463G>C , CM000678.2:g.68737463G>C	GRCh38
NC_000016.9:g.68771366G>C , CM000678.1:g.68771366G>C	GRCh37
NC_000016.8:g.67328867G>C	NCBI36
NG_008021.1:g.5172G>C , LRG_301:g.5172G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000261769.10:c.48G>C MANE Select	ENSP00000261769.4:p.Gln16His
ENST00000261769.9:c.48G>C	ENSP00000261769.4:p.Gln16His
ENST00000422392.6:c.48G>C	ENSP00000414946.2:p.Gln16His
ENST00000566510.5:c.48G>C	ENSP00000458139.1:p.Gln16His
ENST00000566612.5:c.48G>C	ENSP00000454782.1:p.Gln16His
ENST00000611625.4:c.48G>C	ENSP00000481063.1:p.Gln16His
ENST00000612417.4:c.48G>C	ENSP00000478360.1:p.Gln16His
ENST00000621016.4:c.48G>C	ENSP00000480664.1:p.Gln16His
NM_004360.3:c.48G>C , LRG_301t1:c.48G>C	NP_004351.1:p.Gln16His
NM_001317184.1:c.48G>C	NP_001304113.1:p.Gln16His
NM_001317185.1:c.-1568G>C	NP_001304114.1:n.-1568G>C
NM_001317186.1:c.-1772G>C	NP_001304115.1:n.-1772G>C
NM_004360.4:c.48G>C	NP_004351.1:p.Gln16His
NM_004360.5:c.48G>C MANE Select	NP_004351.1:p.Gln16His
NM_001317184.2:c.48G>C	NP_001304113.1:p.Gln16His
NM_001317185.2:c.-1568G>C	NP_001304114.1:n.-1568G>C
NM_001317186.2:c.-1772G>C	NP_001304115.1:n.-1772G>C