Canonical Allele Identifier: CA16042157

Gene: CDH1

Linked Data

• ClinVar Variation Id: 371806
• ClinVar RCV Id: RCV003328334 ; RCV003477907
• dbSNP Id: rs1057517542
• MyVariant Identifiers: chr16:g.68863556G>A (hg19) ; chr16:g.68829653G>A (hg38)
• ERepo: CA16042157/MONDO:0007648/007 ; CA16042157/MONDO:0100488/007

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68829653G>A , CM000678.2:g.68829653G>A	GRCh38
NC_000016.9:g.68863556G>A , CM000678.1:g.68863556G>A	GRCh37
NC_000016.8:g.67421057G>A	NCBI36
NG_008021.1:g.97362G>A , LRG_301:g.97362G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000261769.10:c.2296-1G>A MANE Select	ENSP00000261769.4:n.2296-1G>A
ENST00000261769.9:c.2296-1G>A	ENSP00000261769.4:n.2296-1G>A
ENST00000422392.6:c.2113-1G>A	ENSP00000414946.2:n.2113-1G>A
ENST00000562118.1:n.514-1G>A
ENST00000562836.5:n.2367-1G>A
ENST00000566510.5:c.*962-1G>A	ENSP00000458139.1:n.*962-1G>A
ENST00000566612.5:c.*536-1G>A	ENSP00000454782.1:n.*536-1G>A
ENST00000611625.4:c.2359-1G>A	ENSP00000481063.1:n.2359-1G>A
ENST00000612417.4:c.1853+3099G>A	ENSP00000478360.1:n.1853+3099G>A
ENST00000621016.4:c.1866-4550G>A	ENSP00000480664.1:n.1866-4550G>A
NM_004360.3:c.2296-1G>A , LRG_301t1:c.2296-1G>A	NP_004351.1:n.2296-1G>A
XM_011523488.1:c.1561-1G>A	XP_011521790.1:n.1561-1G>A
XM_011523489.1:c.1561-1G>A	XP_011521791.1:n.1561-1G>A
NM_001317184.1:c.2113-1G>A	NP_001304113.1:n.2113-1G>A
NM_001317185.1:c.748-1G>A	NP_001304114.1:n.748-1G>A
NM_001317186.1:c.331-1G>A	NP_001304115.1:n.331-1G>A
NM_004360.4:c.2296-1G>A	NP_004351.1:n.2296-1G>A
NM_004360.5:c.2296-1G>A MANE Select	NP_004351.1:n.2296-1G>A
NM_001317184.2:c.2113-1G>A	NP_001304113.1:n.2113-1G>A
NM_001317185.2:c.748-1G>A	NP_001304114.1:n.748-1G>A
NM_001317186.2:c.331-1G>A	NP_001304115.1:n.331-1G>A