Canonical Allele Identifier: CA496393028

Gene: CDH1

Linked Data

• dbSNP Id: rs2152143874
• MyVariant Identifiers: chr16:g.68867222A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68833319A>T , CM000678.2:g.68833319A>T	GRCh38
NC_000016.9:g.68867222A>T , CM000678.1:g.68867222A>T	GRCh37
NC_000016.8:g.67424723A>T	NCBI36
NG_008021.1:g.101028A>T , LRG_301:g.101028A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261769.10:c.2469A>T MANE Select	ENSP00000261769.4:p.Thr823=
ENST00000261769.9:c.2469A>T	ENSP00000261769.4:p.Thr823=
ENST00000422392.6:c.2286A>T	ENSP00000414946.2:p.Thr762=
ENST00000562118.1:n.687A>T
ENST00000562836.5:n.2540A>T
ENST00000566510.5:c.*1135A>T	ENSP00000458139.1:n.*1135A>T
ENST00000566612.5:c.*709A>T	ENSP00000454782.1:n.*709A>T
ENST00000611625.4:c.2532A>T	ENSP00000481063.1:p.Thr844=
ENST00000612417.4:c.1854-872A>T	ENSP00000478360.1:n.1854-872A>T
ENST00000621016.4:c.1866-884A>T	ENSP00000480664.1:n.1866-884A>T
NM_004360.3:c.2469A>T , LRG_301t1:c.2469A>T	NP_004351.1:p.Thr823=
XM_011523488.1:c.1734A>T	XP_011521790.1:p.Thr578=
XM_011523489.1:c.1734A>T	XP_011521791.1:p.Thr578=
NM_001317184.1:c.2286A>T	NP_001304113.1:p.Thr762=
NM_001317185.1:c.921A>T	NP_001304114.1:p.Thr307=
NM_001317186.1:c.504A>T	NP_001304115.1:p.Thr168=
NM_004360.4:c.2469A>T	NP_004351.1:p.Thr823=
NM_004360.5:c.2469A>T MANE Select	NP_004351.1:p.Thr823=
NM_001317184.2:c.2286A>T	NP_001304113.1:p.Thr762=
NM_001317185.2:c.921A>T	NP_001304114.1:p.Thr307=
NM_001317186.2:c.504A>T	NP_001304115.1:p.Thr168=