Canonical Allele Identifier: CA396470763

Gene: CDH1

Linked Data

• dbSNP Id: rs2152142220
• MyVariant Identifiers: chr16:g.68863564A>T (hg19) ; chr16:g.68829661A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68829661A>T , CM000678.2:g.68829661A>T	GRCh38
NC_000016.9:g.68863564A>T , CM000678.1:g.68863564A>T	GRCh37
NC_000016.8:g.67421065A>T	NCBI36
NG_008021.1:g.97370A>T , LRG_301:g.97370A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000261769.10:c.2303A>T MANE Select	ENSP00000261769.4:p.Asp768Val
ENST00000261769.9:c.2303A>T	ENSP00000261769.4:p.Asp768Val
ENST00000422392.6:c.2120A>T	ENSP00000414946.2:p.Asp707Val
ENST00000562118.1:n.521A>T
ENST00000562836.5:n.2374A>T
ENST00000566510.5:c.*969A>T	ENSP00000458139.1:n.*969A>T
ENST00000566612.5:c.*543A>T	ENSP00000454782.1:n.*543A>T
ENST00000611625.4:c.2366A>T	ENSP00000481063.1:p.Asp789Val
ENST00000612417.4:c.1853+3107A>T	ENSP00000478360.1:n.1853+3107A>T
ENST00000621016.4:c.1866-4542A>T	ENSP00000480664.1:n.1866-4542A>T
NM_004360.3:c.2303A>T , LRG_301t1:c.2303A>T	NP_004351.1:p.Asp768Val
XM_011523488.1:c.1568A>T	XP_011521790.1:p.Asp523Val
XM_011523489.1:c.1568A>T	XP_011521791.1:p.Asp523Val
NM_001317184.1:c.2120A>T	NP_001304113.1:p.Asp707Val
NM_001317185.1:c.755A>T	NP_001304114.1:p.Asp252Val
NM_001317186.1:c.338A>T	NP_001304115.1:p.Asp113Val
NM_004360.4:c.2303A>T	NP_004351.1:p.Asp768Val
NM_004360.5:c.2303A>T MANE Select	NP_004351.1:p.Asp768Val
NM_001317184.2:c.2120A>T	NP_001304113.1:p.Asp707Val
NM_001317185.2:c.755A>T	NP_001304114.1:p.Asp252Val
NM_001317186.2:c.338A>T	NP_001304115.1:p.Asp113Val