Canonical Allele Identifier: CA396470758

Gene: CDH1

Linked Data

• dbSNP Id: rs786201999
• MyVariant Identifiers: chr16:g.68863563G>T (hg19) ; chr16:g.68829660G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68829660G>T , CM000678.2:g.68829660G>T	GRCh38
NC_000016.9:g.68863563G>T , CM000678.1:g.68863563G>T	GRCh37
NC_000016.8:g.67421064G>T	NCBI36
NG_008021.1:g.97369G>T , LRG_301:g.97369G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000261769.10:c.2302G>T MANE Select	ENSP00000261769.4:p.Asp768Tyr
ENST00000261769.9:c.2302G>T	ENSP00000261769.4:p.Asp768Tyr
ENST00000422392.6:c.2119G>T	ENSP00000414946.2:p.Asp707Tyr
ENST00000562118.1:n.520G>T
ENST00000562836.5:n.2373G>T
ENST00000566510.5:c.*968G>T	ENSP00000458139.1:n.*968G>T
ENST00000566612.5:c.*542G>T	ENSP00000454782.1:n.*542G>T
ENST00000611625.4:c.2365G>T	ENSP00000481063.1:p.Asp789Tyr
ENST00000612417.4:c.1853+3106G>T	ENSP00000478360.1:n.1853+3106G>T
ENST00000621016.4:c.1866-4543G>T	ENSP00000480664.1:n.1866-4543G>T
NM_004360.3:c.2302G>T , LRG_301t1:c.2302G>T	NP_004351.1:p.Asp768Tyr
XM_011523488.1:c.1567G>T	XP_011521790.1:p.Asp523Tyr
XM_011523489.1:c.1567G>T	XP_011521791.1:p.Asp523Tyr
NM_001317184.1:c.2119G>T	NP_001304113.1:p.Asp707Tyr
NM_001317185.1:c.754G>T	NP_001304114.1:p.Asp252Tyr
NM_001317186.1:c.337G>T	NP_001304115.1:p.Asp113Tyr
NM_004360.4:c.2302G>T	NP_004351.1:p.Asp768Tyr
NM_004360.5:c.2302G>T MANE Select	NP_004351.1:p.Asp768Tyr
NM_001317184.2:c.2119G>T	NP_001304113.1:p.Asp707Tyr
NM_001317185.2:c.754G>T	NP_001304114.1:p.Asp252Tyr
NM_001317186.2:c.337G>T	NP_001304115.1:p.Asp113Tyr