Canonical Allele Identifier: CA919732112

Gene: CDH1

Linked Data

• dbSNP Id: rs1596965939

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68823541_68823547del , CM000678.2:g.68823541_68823547del	GRCh38
NC_000016.9:g.68857444_68857450del , CM000678.1:g.68857444_68857450del	GRCh37
NC_000016.8:g.67414945_67414951del	NCBI36
NG_008021.1:g.91250_91256del , LRG_301:g.91250_91256del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261769.10:c.2079_2085del MANE Select	ENSP00000261769.4:p.Val694GlyfsTer26
ENST00000261769.9:c.2079_2085del	ENSP00000261769.4:p.Val694GlyfsTer26
ENST00000422392.6:c.1896_1902del	ENSP00000414946.2:p.Val633GlyfsTer26
ENST00000562118.1:n.297_303del
ENST00000562836.5:n.2150_2156del
ENST00000566510.5:c.*745_*751del	ENSP00000458139.1:n.*745_*751del
ENST00000566612.5:c.*319_*325del	ENSP00000454782.1:n.*319_*325del
ENST00000611625.4:c.2142_2148del	ENSP00000481063.1:p.Val715GlyfsTer26
ENST00000612417.4:c.1830+1422_1830+1428del	ENSP00000478360.1:n.1830+1422_1830+1428del
ENST00000621016.4:c.1865+1387_1865+1393del	ENSP00000480664.1:n.1865+1387_1865+1393del
NM_004360.3:c.2079_2085del , LRG_301t1:c.2079_2085del	NP_004351.1:p.Val694GlyfsTer26
XM_011523488.1:c.1344_1350del	XP_011521790.1:p.Val449GlyfsTer26
XM_011523489.1:c.1344_1350del	XP_011521791.1:p.Val449GlyfsTer26
NM_001317184.1:c.1896_1902del	NP_001304113.1:p.Val633GlyfsTer26
NM_001317185.1:c.531_537del	NP_001304114.1:p.Val178GlyfsTer26
NM_001317186.1:c.114_120del	NP_001304115.1:p.Val39GlyfsTer26
NM_004360.4:c.2079_2085del	NP_004351.1:p.Val694GlyfsTer26
NM_004360.5:c.2079_2085del MANE Select	NP_004351.1:p.Val694GlyfsTer26
NM_001317184.2:c.1896_1902del	NP_001304113.1:p.Val633GlyfsTer26
NM_001317185.2:c.531_537del	NP_001304114.1:p.Val178GlyfsTer26
NM_001317186.2:c.114_120del	NP_001304115.1:p.Val39GlyfsTer26