Canonical Allele Identifier: CA396471274

Gene: CDH1

Linked Data

• ClinVar Variation Id: 656429
• ClinVar RCV Id: RCV000812843
• dbSNP Id: rs1481419710
• MyVariant Identifiers: chr16:g.68863675A>T (hg19) ; chr16:g.68829772A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68829772A>T , CM000678.2:g.68829772A>T	GRCh38
NC_000016.9:g.68863675A>T , CM000678.1:g.68863675A>T	GRCh37
NC_000016.8:g.67421176A>T	NCBI36
NG_008021.1:g.97481A>T , LRG_301:g.97481A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261769.10:c.2414A>T MANE Select	ENSP00000261769.4:p.Asp805Val
ENST00000261769.9:c.2414A>T	ENSP00000261769.4:p.Asp805Val
ENST00000422392.6:c.2231A>T	ENSP00000414946.2:p.Asp744Val
ENST00000562118.1:n.632A>T
ENST00000562836.5:n.2485A>T
ENST00000566510.5:c.*1080A>T	ENSP00000458139.1:n.*1080A>T
ENST00000566612.5:c.*654A>T	ENSP00000454782.1:n.*654A>T
ENST00000611625.4:c.2477A>T	ENSP00000481063.1:p.Asp826Val
ENST00000612417.4:c.1853+3218A>T	ENSP00000478360.1:n.1853+3218A>T
ENST00000621016.4:c.1866-4431A>T	ENSP00000480664.1:n.1866-4431A>T
NM_004360.3:c.2414A>T , LRG_301t1:c.2414A>T	NP_004351.1:p.Asp805Val
XM_011523488.1:c.1679A>T	XP_011521790.1:p.Asp560Val
XM_011523489.1:c.1679A>T	XP_011521791.1:p.Asp560Val
NM_001317184.1:c.2231A>T	NP_001304113.1:p.Asp744Val
NM_001317185.1:c.866A>T	NP_001304114.1:p.Asp289Val
NM_001317186.1:c.449A>T	NP_001304115.1:p.Asp150Val
NM_004360.4:c.2414A>T	NP_004351.1:p.Asp805Val
NM_004360.5:c.2414A>T MANE Select	NP_004351.1:p.Asp805Val
NM_001317184.2:c.2231A>T	NP_001304113.1:p.Asp744Val
NM_001317185.2:c.866A>T	NP_001304114.1:p.Asp289Val
NM_001317186.2:c.449A>T	NP_001304115.1:p.Asp150Val