Canonical Allele Identifier: CA283312663

Gene: CDH1 FTLP14

Linked Data

• dbSNP Id: rs186435674
• gnomAD v4: 16-68823025-C-A
• MyVariant Identifiers: chr16:g.68856928C>A (hg19) ; chr16:g.68823025C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68823025C>A , CM000678.2:g.68823025C>A	GRCh38
NC_000016.9:g.68856928C>A , CM000678.1:g.68856928C>A	GRCh37
NC_000016.8:g.67414429C>A	NCBI36
NG_008021.1:g.90734C>A , LRG_301:g.90734C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261769.10:c.1937-374C>A (CDH1) MANE Select	ENSP00000261769.4:n.1937-374C>A
ENST00000261769.9:c.1937-374C>A (CDH1)	ENSP00000261769.4:n.1937-374C>A
ENST00000422392.6:c.1754-374C>A (CDH1)	ENSP00000414946.2:n.1754-374C>A
ENST00000562087.2:n.439C>A (FTLP14)
ENST00000562836.5:n.2008-374C>A (CDH1)
ENST00000566510.5:c.*603-374C>A (CDH1)	ENSP00000458139.1:n.*603-374C>A
ENST00000566612.5:c.*177-374C>A (CDH1)	ENSP00000454782.1:n.*177-374C>A
ENST00000611625.4:c.2000-374C>A (CDH1)	ENSP00000481063.1:n.2000-374C>A
ENST00000612417.4:c.1830+906C>A (CDH1)	ENSP00000478360.1:n.1830+906C>A
ENST00000621016.4:c.1865+871C>A (CDH1)	ENSP00000480664.1:n.1865+871C>A
NM_004360.3:c.1937-374C>A , LRG_301t1:c.1937-374C>A (CDH1)	NP_004351.1:n.1937-374C>A
XM_011523488.1:c.1202-374C>A (CDH1)	XP_011521790.1:n.1202-374C>A
XM_011523489.1:c.1202-374C>A (CDH1)	XP_011521791.1:n.1202-374C>A
NM_001317184.1:c.1754-374C>A (CDH1)	NP_001304113.1:n.1754-374C>A
NM_001317185.1:c.389-374C>A (CDH1)	NP_001304114.1:n.389-374C>A
NM_001317186.1:c.-29-374C>A (CDH1)	NP_001304115.1:n.-29-374C>A
NM_004360.4:c.1937-374C>A (CDH1)	NP_004351.1:n.1937-374C>A
NM_004360.5:c.1937-374C>A (CDH1) MANE Select	NP_004351.1:n.1937-374C>A
NM_001317184.2:c.1754-374C>A (CDH1)	NP_001304113.1:n.1754-374C>A
NM_001317185.2:c.389-374C>A (CDH1)	NP_001304114.1:n.389-374C>A
NM_001317186.2:c.-29-374C>A (CDH1)	NP_001304115.1:n.-29-374C>A