Canonical Allele Identifier: CA396472930

Gene: CDH1

Linked Data

• dbSNP Id: rs2152144267
• MyVariant Identifiers: chr16:g.68867395A>C (hg19) ; chr16:g.68833492A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68833492A>C , CM000678.2:g.68833492A>C	GRCh38
NC_000016.9:g.68867395A>C , CM000678.1:g.68867395A>C	GRCh37
NC_000016.8:g.67424896A>C	NCBI36
NG_008021.1:g.101201A>C , LRG_301:g.101201A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261769.10:c.2642A>C MANE Select	ENSP00000261769.4:p.Asp881Ala
ENST00000261769.9:c.2642A>C	ENSP00000261769.4:p.Asp881Ala
ENST00000422392.6:c.2459A>C	ENSP00000414946.2:p.Asp820Ala
ENST00000562118.1:n.860A>C
ENST00000562836.5:n.2713A>C
ENST00000566510.5:c.*1308A>C	ENSP00000458139.1:n.*1308A>C
ENST00000566612.5:c.*882A>C	ENSP00000454782.1:n.*882A>C
ENST00000611625.4:c.2705A>C	ENSP00000481063.1:p.Asp902Ala
ENST00000612417.4:c.1854-699A>C	ENSP00000478360.1:n.1854-699A>C
ENST00000621016.4:c.1866-711A>C	ENSP00000480664.1:n.1866-711A>C
NM_004360.3:c.2642A>C , LRG_301t1:c.2642A>C	NP_004351.1:p.Asp881Ala
XM_011523488.1:c.1907A>C	XP_011521790.1:p.Asp636Ala
XM_011523489.1:c.1907A>C	XP_011521791.1:p.Asp636Ala
NM_001317184.1:c.2459A>C	NP_001304113.1:p.Asp820Ala
NM_001317185.1:c.1094A>C	NP_001304114.1:p.Asp365Ala
NM_001317186.1:c.677A>C	NP_001304115.1:p.Asp226Ala
NM_004360.4:c.2642A>C	NP_004351.1:p.Asp881Ala
NM_004360.5:c.2642A>C MANE Select	NP_004351.1:p.Asp881Ala
NM_001317184.2:c.2459A>C	NP_001304113.1:p.Asp820Ala
NM_001317185.2:c.1094A>C	NP_001304114.1:p.Asp365Ala
NM_001317186.2:c.677A>C	NP_001304115.1:p.Asp226Ala