Canonical Allele Identifier: CA396465163

Gene: CDH1

Linked Data

• dbSNP Id: rs876658877
• MyVariant Identifiers: chr16:g.68853253G>T (hg19) ; chr16:g.68819350G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68819350G>T , CM000678.2:g.68819350G>T	GRCh38
NC_000016.9:g.68853253G>T , CM000678.1:g.68853253G>T	GRCh37
NC_000016.8:g.67410754G>T	NCBI36
NG_008021.1:g.87059G>T , LRG_301:g.87059G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261769.10:c.1636G>T MANE Select	ENSP00000261769.4:p.Ala546Ser
ENST00000261769.9:c.1636G>T	ENSP00000261769.4:p.Ala546Ser
ENST00000422392.6:c.1453G>T	ENSP00000414946.2:p.Ala485Ser
ENST00000562836.5:n.1707G>T
ENST00000566510.5:c.*302G>T	ENSP00000458139.1:n.*302G>T
ENST00000566612.5:c.1566-2651G>T	ENSP00000454782.1:n.1566-2651G>T
ENST00000611625.4:c.1699G>T	ENSP00000481063.1:p.Ala567Ser
ENST00000612417.4:c.1636G>T	ENSP00000478360.1:p.Ala546Ser
ENST00000621016.4:c.1636G>T	ENSP00000480664.1:p.Ala546Ser
NM_004360.3:c.1636G>T , LRG_301t1:c.1636G>T	NP_004351.1:p.Ala546Ser
XM_011523488.1:c.901G>T	XP_011521790.1:p.Ala301Ser
XM_011523489.1:c.901G>T	XP_011521791.1:p.Ala301Ser
NM_001317184.1:c.1453G>T	NP_001304113.1:p.Ala485Ser
NM_001317185.1:c.88G>T	NP_001304114.1:p.Ala30Ser
NM_001317186.1:c.-254-2651G>T	NP_001304115.1:n.-254-2651G>T
NM_004360.4:c.1636G>T	NP_004351.1:p.Ala546Ser
NM_004360.5:c.1636G>T MANE Select	NP_004351.1:p.Ala546Ser
NM_001317184.2:c.1453G>T	NP_001304113.1:p.Ala485Ser
NM_001317185.2:c.88G>T	NP_001304114.1:p.Ala30Ser
NM_001317186.2:c.-254-2651G>T	NP_001304115.1:n.-254-2651G>T