Canonical Allele Identifier: CA396470096

Gene: CDH1

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68828296G>C , CM000678.2:g.68828296G>C	GRCh38
NC_000016.9:g.68862199G>C , CM000678.1:g.68862199G>C	GRCh37
NC_000016.8:g.67419700G>C	NCBI36
NG_008021.1:g.96005G>C , LRG_301:g.96005G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261769.10:c.2287G>C MANE Select	ENSP00000261769.4:p.Glu763Gln
ENST00000261769.9:c.2287G>C	ENSP00000261769.4:p.Glu763Gln
ENST00000422392.6:c.2104G>C	ENSP00000414946.2:p.Glu702Gln
ENST00000562118.1:n.505G>C
ENST00000562836.5:n.2358G>C
ENST00000566510.5:c.*953G>C	ENSP00000458139.1:n.*953G>C
ENST00000566612.5:c.*527G>C	ENSP00000454782.1:n.*527G>C
ENST00000611625.4:c.2350G>C	ENSP00000481063.1:p.Glu784Gln
ENST00000612417.4:c.1853+1742G>C	ENSP00000478360.1:n.1853+1742G>C
ENST00000621016.4:c.1866-5907G>C	ENSP00000480664.1:n.1866-5907G>C
NM_004360.3:c.2287G>C , LRG_301t1:c.2287G>C	NP_004351.1:p.Glu763Gln
XM_011523488.1:c.1552G>C	XP_011521790.1:p.Glu518Gln
XM_011523489.1:c.1552G>C	XP_011521791.1:p.Glu518Gln
NM_001317184.1:c.2104G>C	NP_001304113.1:p.Glu702Gln
NM_001317185.1:c.739G>C	NP_001304114.1:p.Glu247Gln
NM_001317186.1:c.322G>C	NP_001304115.1:p.Glu108Gln
NM_004360.4:c.2287G>C	NP_004351.1:p.Glu763Gln
NM_004360.5:c.2287G>C MANE Select	NP_004351.1:p.Glu763Gln
NM_001317184.2:c.2104G>C	NP_001304113.1:p.Glu702Gln
NM_001317185.2:c.739G>C	NP_001304114.1:p.Glu247Gln
NM_001317186.2:c.322G>C	NP_001304115.1:p.Glu108Gln