Canonical Allele Identifier: CA396470938

Gene: CDH1

Linked Data

• dbSNP Id: rs2152142289
• MyVariant Identifiers: chr16:g.68863599C>A (hg19) ; chr16:g.68829696C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68829696C>A , CM000678.2:g.68829696C>A	GRCh38
NC_000016.9:g.68863599C>A , CM000678.1:g.68863599C>A	GRCh37
NC_000016.8:g.67421100C>A	NCBI36
NG_008021.1:g.97405C>A , LRG_301:g.97405C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000261769.10:c.2338C>A MANE Select	ENSP00000261769.4:p.Pro780Thr
ENST00000261769.9:c.2338C>A	ENSP00000261769.4:p.Pro780Thr
ENST00000422392.6:c.2155C>A	ENSP00000414946.2:p.Pro719Thr
ENST00000562118.1:n.556C>A
ENST00000562836.5:n.2409C>A
ENST00000566510.5:c.*1004C>A	ENSP00000458139.1:n.*1004C>A
ENST00000566612.5:c.*578C>A	ENSP00000454782.1:n.*578C>A
ENST00000611625.4:c.2401C>A	ENSP00000481063.1:p.Pro801Thr
ENST00000612417.4:c.1853+3142C>A	ENSP00000478360.1:n.1853+3142C>A
ENST00000621016.4:c.1866-4507C>A	ENSP00000480664.1:n.1866-4507C>A
NM_004360.3:c.2338C>A , LRG_301t1:c.2338C>A	NP_004351.1:p.Pro780Thr
XM_011523488.1:c.1603C>A	XP_011521790.1:p.Pro535Thr
XM_011523489.1:c.1603C>A	XP_011521791.1:p.Pro535Thr
NM_001317184.1:c.2155C>A	NP_001304113.1:p.Pro719Thr
NM_001317185.1:c.790C>A	NP_001304114.1:p.Pro264Thr
NM_001317186.1:c.373C>A	NP_001304115.1:p.Pro125Thr
NM_004360.4:c.2338C>A	NP_004351.1:p.Pro780Thr
NM_004360.5:c.2338C>A MANE Select	NP_004351.1:p.Pro780Thr
NM_001317184.2:c.2155C>A	NP_001304113.1:p.Pro719Thr
NM_001317185.2:c.790C>A	NP_001304114.1:p.Pro264Thr
NM_001317186.2:c.373C>A	NP_001304115.1:p.Pro125Thr