Canonical Allele Identifier: CA396467203

Gene: CDH1

Linked Data

• dbSNP Id: rs2152138567
• MyVariant Identifiers: chr16:g.68856097T>A (hg19) ; chr16:g.68822194T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68822194T>A , CM000678.2:g.68822194T>A	GRCh38
NC_000016.9:g.68856097T>A , CM000678.1:g.68856097T>A	GRCh37
NC_000016.8:g.67413598T>A	NCBI36
NG_008021.1:g.89903T>A , LRG_301:g.89903T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261769.10:c.1905T>A MANE Select	ENSP00000261769.4:p.Ser635Arg
ENST00000261769.9:c.1905T>A	ENSP00000261769.4:p.Ser635Arg
ENST00000422392.6:c.1722T>A	ENSP00000414946.2:p.Ser574Arg
ENST00000562836.5:n.1976T>A
ENST00000566510.5:c.*571T>A	ENSP00000458139.1:n.*571T>A
ENST00000566612.5:c.*145T>A	ENSP00000454782.1:n.*145T>A
ENST00000611625.4:c.1968T>A	ENSP00000481063.1:p.Ser656Arg
ENST00000612417.4:c.1830+75T>A	ENSP00000478360.1:n.1830+75T>A
ENST00000621016.4:c.1865+40T>A	ENSP00000480664.1:n.1865+40T>A
NM_004360.3:c.1905T>A , LRG_301t1:c.1905T>A	NP_004351.1:p.Ser635Arg
XM_011523488.1:c.1170T>A	XP_011521790.1:p.Ser390Arg
XM_011523489.1:c.1170T>A	XP_011521791.1:p.Ser390Arg
NM_001317184.1:c.1722T>A	NP_001304113.1:p.Ser574Arg
NM_001317185.1:c.357T>A	NP_001304114.1:p.Ser119Arg
NM_001317186.1:c.-61T>A	NP_001304115.1:n.-61T>A
NM_004360.4:c.1905T>A	NP_004351.1:p.Ser635Arg
NM_004360.5:c.1905T>A MANE Select	NP_004351.1:p.Ser635Arg
NM_001317184.2:c.1722T>A	NP_001304113.1:p.Ser574Arg
NM_001317185.2:c.357T>A	NP_001304114.1:p.Ser119Arg
NM_001317186.2:c.-61T>A	NP_001304115.1:n.-61T>A