Canonical Allele Identifier: CA496392821

Gene: CDH1

Linked Data

• dbSNP Id: rs786201138
• MyVariant Identifiers: chr16:g.68856061A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68822158A>C , CM000678.2:g.68822158A>C	GRCh38
NC_000016.9:g.68856061A>C , CM000678.1:g.68856061A>C	GRCh37
NC_000016.8:g.67413562A>C	NCBI36
NG_008021.1:g.89867A>C , LRG_301:g.89867A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000261769.10:c.1869A>C MANE Select	ENSP00000261769.4:p.Thr623=
ENST00000261769.9:c.1869A>C	ENSP00000261769.4:p.Thr623=
ENST00000422392.6:c.1686A>C	ENSP00000414946.2:p.Thr562=
ENST00000562836.5:n.1940A>C
ENST00000566510.5:c.*535A>C	ENSP00000458139.1:n.*535A>C
ENST00000566612.5:c.*109A>C	ENSP00000454782.1:n.*109A>C
ENST00000611625.4:c.1932A>C	ENSP00000481063.1:p.Thr644=
ENST00000612417.4:c.1830+39A>C	ENSP00000478360.1:n.1830+39A>C
ENST00000621016.4:c.1865+4A>C	ENSP00000480664.1:n.1865+4A>C
NM_004360.3:c.1869A>C , LRG_301t1:c.1869A>C	NP_004351.1:p.Thr623=
XM_011523488.1:c.1134A>C	XP_011521790.1:p.Thr378=
XM_011523489.1:c.1134A>C	XP_011521791.1:p.Thr378=
NM_001317184.1:c.1686A>C	NP_001304113.1:p.Thr562=
NM_001317185.1:c.321A>C	NP_001304114.1:p.Thr107=
NM_001317186.1:c.-97A>C	NP_001304115.1:n.-97A>C
NM_004360.4:c.1869A>C	NP_004351.1:p.Thr623=
NM_004360.5:c.1869A>C MANE Select	NP_004351.1:p.Thr623=
NM_001317184.2:c.1686A>C	NP_001304113.1:p.Thr562=
NM_001317185.2:c.321A>C	NP_001304114.1:p.Thr107=
NM_001317186.2:c.-97A>C	NP_001304115.1:n.-97A>C