Canonical Allele Identifier: CA496392619

Gene: CDH1

Linked Data

• dbSNP Id: rs2152138389
• MyVariant Identifiers: chr16:g.68856019T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68822116T>A , CM000678.2:g.68822116T>A	GRCh38
NC_000016.9:g.68856019T>A , CM000678.1:g.68856019T>A	GRCh37
NC_000016.8:g.67413520T>A	NCBI36
NG_008021.1:g.89825T>A , LRG_301:g.89825T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261769.10:c.1827T>A MANE Select	ENSP00000261769.4:p.Pro609=
ENST00000261769.9:c.1827T>A	ENSP00000261769.4:p.Pro609=
ENST00000422392.6:c.1644T>A	ENSP00000414946.2:p.Pro548=
ENST00000562836.5:n.1898T>A
ENST00000566510.5:c.*493T>A	ENSP00000458139.1:n.*493T>A
ENST00000566612.5:c.*67T>A	ENSP00000454782.1:n.*67T>A
ENST00000611625.4:c.1890T>A	ENSP00000481063.1:p.Pro630=
ENST00000612417.4:c.1827T>A	ENSP00000478360.1:p.Pro609=
ENST00000621016.4:c.1827T>A	ENSP00000480664.1:p.Pro609=
NM_004360.3:c.1827T>A , LRG_301t1:c.1827T>A	NP_004351.1:p.Pro609=
XM_011523488.1:c.1092T>A	XP_011521790.1:p.Pro364=
XM_011523489.1:c.1092T>A	XP_011521791.1:p.Pro364=
NM_001317184.1:c.1644T>A	NP_001304113.1:p.Pro548=
NM_001317185.1:c.279T>A	NP_001304114.1:p.Pro93=
NM_001317186.1:c.-139T>A	NP_001304115.1:n.-139T>A
NM_004360.4:c.1827T>A	NP_004351.1:p.Pro609=
NM_004360.5:c.1827T>A MANE Select	NP_004351.1:p.Pro609=
NM_001317184.2:c.1644T>A	NP_001304113.1:p.Pro548=
NM_001317185.2:c.279T>A	NP_001304114.1:p.Pro93=
NM_001317186.2:c.-139T>A	NP_001304115.1:n.-139T>A