Canonical Allele Identifier: CA496156637

Gene: CDH1 FTLP14

Linked Data

• gnomAD v4: 16-68823016-A-C
• MyVariant Identifiers: chr16:g.68856919A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68823016A>C , CM000678.2:g.68823016A>C	GRCh38
NC_000016.9:g.68856919A>C , CM000678.1:g.68856919A>C	GRCh37
NC_000016.8:g.67414420A>C	NCBI36
NG_008021.1:g.90725A>C , LRG_301:g.90725A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261769.10:c.1937-383A>C (CDH1) MANE Select	ENSP00000261769.4:n.1937-383A>C
ENST00000261769.9:c.1937-383A>C (CDH1)	ENSP00000261769.4:n.1937-383A>C
ENST00000422392.6:c.1754-383A>C (CDH1)	ENSP00000414946.2:n.1754-383A>C
ENST00000562087.2:n.430A>C (FTLP14)
ENST00000562836.5:n.2008-383A>C (CDH1)
ENST00000566510.5:c.*603-383A>C (CDH1)	ENSP00000458139.1:n.*603-383A>C
ENST00000566612.5:c.*177-383A>C (CDH1)	ENSP00000454782.1:n.*177-383A>C
ENST00000611625.4:c.2000-383A>C (CDH1)	ENSP00000481063.1:n.2000-383A>C
ENST00000612417.4:c.1830+897A>C (CDH1)	ENSP00000478360.1:n.1830+897A>C
ENST00000621016.4:c.1865+862A>C (CDH1)	ENSP00000480664.1:n.1865+862A>C
NM_004360.3:c.1937-383A>C , LRG_301t1:c.1937-383A>C (CDH1)	NP_004351.1:n.1937-383A>C
XM_011523488.1:c.1202-383A>C (CDH1)	XP_011521790.1:n.1202-383A>C
XM_011523489.1:c.1202-383A>C (CDH1)	XP_011521791.1:n.1202-383A>C
NM_001317184.1:c.1754-383A>C (CDH1)	NP_001304113.1:n.1754-383A>C
NM_001317185.1:c.389-383A>C (CDH1)	NP_001304114.1:n.389-383A>C
NM_001317186.1:c.-29-383A>C (CDH1)	NP_001304115.1:n.-29-383A>C
NM_004360.4:c.1937-383A>C (CDH1)	NP_004351.1:n.1937-383A>C
NM_004360.5:c.1937-383A>C (CDH1) MANE Select	NP_004351.1:n.1937-383A>C
NM_001317184.2:c.1754-383A>C (CDH1)	NP_001304113.1:n.1754-383A>C
NM_001317185.2:c.389-383A>C (CDH1)	NP_001304114.1:n.389-383A>C
NM_001317186.2:c.-29-383A>C (CDH1)	NP_001304115.1:n.-29-383A>C