Canonical Allele Identifier: CA496393218

Gene: CDH1

Linked Data

• dbSNP Id: rs2152144186
• MyVariant Identifiers: chr16:g.68867363G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68833460G>A , CM000678.2:g.68833460G>A	GRCh38
NC_000016.9:g.68867363G>A , CM000678.1:g.68867363G>A	GRCh37
NC_000016.8:g.67424864G>A	NCBI36
NG_008021.1:g.101169G>A , LRG_301:g.101169G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261769.10:c.2610G>A MANE Select	ENSP00000261769.4:p.Lys870=
ENST00000261769.9:c.2610G>A	ENSP00000261769.4:p.Lys870=
ENST00000422392.6:c.2427G>A	ENSP00000414946.2:p.Lys809=
ENST00000562118.1:n.828G>A
ENST00000562836.5:n.2681G>A
ENST00000566510.5:c.*1276G>A	ENSP00000458139.1:n.*1276G>A
ENST00000566612.5:c.*850G>A	ENSP00000454782.1:n.*850G>A
ENST00000611625.4:c.2673G>A	ENSP00000481063.1:p.Lys891=
ENST00000612417.4:c.1854-731G>A	ENSP00000478360.1:n.1854-731G>A
ENST00000621016.4:c.1866-743G>A	ENSP00000480664.1:n.1866-743G>A
NM_004360.3:c.2610G>A , LRG_301t1:c.2610G>A	NP_004351.1:p.Lys870=
XM_011523488.1:c.1875G>A	XP_011521790.1:p.Lys625=
XM_011523489.1:c.1875G>A	XP_011521791.1:p.Lys625=
NM_001317184.1:c.2427G>A	NP_001304113.1:p.Lys809=
NM_001317185.1:c.1062G>A	NP_001304114.1:p.Lys354=
NM_001317186.1:c.645G>A	NP_001304115.1:p.Lys215=
NM_004360.4:c.2610G>A	NP_004351.1:p.Lys870=
NM_004360.5:c.2610G>A MANE Select	NP_004351.1:p.Lys870=
NM_001317184.2:c.2427G>A	NP_001304113.1:p.Lys809=
NM_001317185.2:c.1062G>A	NP_001304114.1:p.Lys354=
NM_001317186.2:c.645G>A	NP_001304115.1:p.Lys215=