Canonical Allele Identifier: CA396470943

Gene: CDH1

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000261769.10:c.2338C>T MANE Select	ENSP00000261769.4:p.Pro780Ser
ENST00000261769.9:c.2338C>T	ENSP00000261769.4:p.Pro780Ser
ENST00000422392.6:c.2155C>T	ENSP00000414946.2:p.Pro719Ser
ENST00000562118.1:n.556C>T
ENST00000562836.5:n.2409C>T
ENST00000566510.5:c.*1004C>T	ENSP00000458139.1:n.*1004C>T
ENST00000566612.5:c.*578C>T	ENSP00000454782.1:n.*578C>T
ENST00000611625.4:c.2401C>T	ENSP00000481063.1:p.Pro801Ser
ENST00000612417.4:c.1853+3142C>T	ENSP00000478360.1:n.1853+3142C>T
ENST00000621016.4:c.1866-4507C>T	ENSP00000480664.1:n.1866-4507C>T
NM_004360.3:c.2338C>T , LRG_301t1:c.2338C>T	NP_004351.1:p.Pro780Ser
XM_011523488.1:c.1603C>T	XP_011521790.1:p.Pro535Ser
XM_011523489.1:c.1603C>T	XP_011521791.1:p.Pro535Ser
NM_001317184.1:c.2155C>T	NP_001304113.1:p.Pro719Ser
NM_001317185.1:c.790C>T	NP_001304114.1:p.Pro264Ser
NM_001317186.1:c.373C>T	NP_001304115.1:p.Pro125Ser
NM_004360.4:c.2338C>T	NP_004351.1:p.Pro780Ser
NM_004360.5:c.2338C>T MANE Select	NP_004351.1:p.Pro780Ser
NM_001317184.2:c.2155C>T	NP_001304113.1:p.Pro719Ser
NM_001317185.2:c.790C>T	NP_001304114.1:p.Pro264Ser
NM_001317186.2:c.373C>T	NP_001304115.1:p.Pro125Ser