Canonical Allele Identifier: CA723142049

Gene: CDH1

Linked Data

• dbSNP Id: rs1346093555
• gnomAD v3: 16-68827781-A-C
• gnomAD v4: 16-68827781-A-C
• MyVariant Identifiers: chr16:g.68861684A>C (hg19) ; chr16:g.68827781A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68827781A>C , CM000678.2:g.68827781A>C	GRCh38
NC_000016.9:g.68861684A>C , CM000678.1:g.68861684A>C	GRCh37
NC_000016.8:g.67419185A>C	NCBI36
NG_008021.1:g.95490A>C , LRG_301:g.95490A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000261769.10:c.2165-393A>C MANE Select	ENSP00000261769.4:n.2165-393A>C
ENST00000261769.9:c.2165-393A>C	ENSP00000261769.4:n.2165-393A>C
ENST00000422392.6:c.1982-393A>C	ENSP00000414946.2:n.1982-393A>C
ENST00000562118.1:n.383-393A>C
ENST00000562836.5:n.2236-393A>C
ENST00000566510.5:c.*831-393A>C	ENSP00000458139.1:n.*831-393A>C
ENST00000566612.5:c.*405-393A>C	ENSP00000454782.1:n.*405-393A>C
ENST00000611625.4:c.2228-393A>C	ENSP00000481063.1:n.2228-393A>C
ENST00000612417.4:c.1853+1227A>C	ENSP00000478360.1:n.1853+1227A>C
ENST00000621016.4:c.1865+5627A>C	ENSP00000480664.1:n.1865+5627A>C
NM_004360.3:c.2165-393A>C , LRG_301t1:c.2165-393A>C	NP_004351.1:n.2165-393A>C
XM_011523488.1:c.1430-393A>C	XP_011521790.1:n.1430-393A>C
XM_011523489.1:c.1430-393A>C	XP_011521791.1:n.1430-393A>C
NM_001317184.1:c.1982-393A>C	NP_001304113.1:n.1982-393A>C
NM_001317185.1:c.617-393A>C	NP_001304114.1:n.617-393A>C
NM_001317186.1:c.200-393A>C	NP_001304115.1:n.200-393A>C
NM_004360.4:c.2165-393A>C	NP_004351.1:n.2165-393A>C
NM_004360.5:c.2165-393A>C MANE Select	NP_004351.1:n.2165-393A>C
NM_001317184.2:c.1982-393A>C	NP_001304113.1:n.1982-393A>C
NM_001317185.2:c.617-393A>C	NP_001304114.1:n.617-393A>C
NM_001317186.2:c.200-393A>C	NP_001304115.1:n.200-393A>C