Canonical Allele Identifier: CA396467176

Gene: CDH1

Linked Data

• dbSNP Id: rs587782850
• MyVariant Identifiers: chr16:g.68856090G>C (hg19) ; chr16:g.68822187G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68822187G>C , CM000678.2:g.68822187G>C	GRCh38
NC_000016.9:g.68856090G>C , CM000678.1:g.68856090G>C	GRCh37
NC_000016.8:g.67413591G>C	NCBI36
NG_008021.1:g.89896G>C , LRG_301:g.89896G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000261769.10:c.1898G>C MANE Select	ENSP00000261769.4:p.Gly633Ala
ENST00000261769.9:c.1898G>C	ENSP00000261769.4:p.Gly633Ala
ENST00000422392.6:c.1715G>C	ENSP00000414946.2:p.Gly572Ala
ENST00000562836.5:n.1969G>C
ENST00000566510.5:c.*564G>C	ENSP00000458139.1:n.*564G>C
ENST00000566612.5:c.*138G>C	ENSP00000454782.1:n.*138G>C
ENST00000611625.4:c.1961G>C	ENSP00000481063.1:p.Gly654Ala
ENST00000612417.4:c.1830+68G>C	ENSP00000478360.1:n.1830+68G>C
ENST00000621016.4:c.1865+33G>C	ENSP00000480664.1:n.1865+33G>C
NM_004360.3:c.1898G>C , LRG_301t1:c.1898G>C	NP_004351.1:p.Gly633Ala
XM_011523488.1:c.1163G>C	XP_011521790.1:p.Gly388Ala
XM_011523489.1:c.1163G>C	XP_011521791.1:p.Gly388Ala
NM_001317184.1:c.1715G>C	NP_001304113.1:p.Gly572Ala
NM_001317185.1:c.350G>C	NP_001304114.1:p.Gly117Ala
NM_001317186.1:c.-68G>C	NP_001304115.1:n.-68G>C
NM_004360.4:c.1898G>C	NP_004351.1:p.Gly633Ala
NM_004360.5:c.1898G>C MANE Select	NP_004351.1:p.Gly633Ala
NM_001317184.2:c.1715G>C	NP_001304113.1:p.Gly572Ala
NM_001317185.2:c.350G>C	NP_001304114.1:p.Gly117Ala
NM_001317186.2:c.-68G>C	NP_001304115.1:n.-68G>C