Canonical Allele Identifier: CA396462846

Gene: CDH1

Linked Data

• dbSNP Id: rs1355592880
• COSMIC: COSM3511253
• MyVariant Identifiers: chr16:g.68849478C>T (hg19) ; chr16:g.68815575C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68815575C>T , CM000678.2:g.68815575C>T	GRCh38
NC_000016.9:g.68849478C>T , CM000678.1:g.68849478C>T	GRCh37
NC_000016.8:g.67406979C>T	NCBI36
NG_008021.1:g.83284C>T , LRG_301:g.83284C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000261769.10:c.1381C>T MANE Select	ENSP00000261769.4:p.Pro461Ser
ENST00000261769.9:c.1381C>T	ENSP00000261769.4:p.Pro461Ser
ENST00000422392.6:c.1198C>T	ENSP00000414946.2:p.Pro400Ser
ENST00000562836.5:n.1452C>T
ENST00000566510.5:c.*47C>T	ENSP00000458139.1:n.*47C>T
ENST00000566612.5:c.1381C>T	ENSP00000454782.1:p.Pro461Ser
ENST00000611625.4:c.1444C>T	ENSP00000481063.1:p.Pro482Ser
ENST00000612417.4:c.1381C>T	ENSP00000478360.1:p.Pro461Ser
ENST00000621016.4:c.1381C>T	ENSP00000480664.1:p.Pro461Ser
NM_004360.3:c.1381C>T , LRG_301t1:c.1381C>T	NP_004351.1:p.Pro461Ser
XM_011523488.1:c.646C>T	XP_011521790.1:p.Pro216Ser
XM_011523489.1:c.646C>T	XP_011521791.1:p.Pro216Ser
NM_001317184.1:c.1198C>T	NP_001304113.1:p.Pro400Ser
NM_001317185.1:c.-168C>T	NP_001304114.1:n.-168C>T
NM_001317186.1:c.-439C>T	NP_001304115.1:n.-439C>T
NM_004360.4:c.1381C>T	NP_004351.1:p.Pro461Ser
NM_004360.5:c.1381C>T MANE Select	NP_004351.1:p.Pro461Ser
NM_001317184.2:c.1198C>T	NP_001304113.1:p.Pro400Ser
NM_001317185.2:c.-168C>T	NP_001304114.1:n.-168C>T
NM_001317186.2:c.-439C>T	NP_001304115.1:n.-439C>T