Canonical Allele Identifier: CA396471261

Gene: CDH1

Linked Data

• dbSNP Id: rs1596972823
• MyVariant Identifiers: chr16:g.68863672C>T (hg19) ; chr16:g.68829769C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68829769C>T , CM000678.2:g.68829769C>T	GRCh38
NC_000016.9:g.68863672C>T , CM000678.1:g.68863672C>T	GRCh37
NC_000016.8:g.67421173C>T	NCBI36
NG_008021.1:g.97478C>T , LRG_301:g.97478C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261769.10:c.2411C>T MANE Select	ENSP00000261769.4:p.Pro804Leu
ENST00000261769.9:c.2411C>T	ENSP00000261769.4:p.Pro804Leu
ENST00000422392.6:c.2228C>T	ENSP00000414946.2:p.Pro743Leu
ENST00000562118.1:n.629C>T
ENST00000562836.5:n.2482C>T
ENST00000566510.5:c.*1077C>T	ENSP00000458139.1:n.*1077C>T
ENST00000566612.5:c.*651C>T	ENSP00000454782.1:n.*651C>T
ENST00000611625.4:c.2474C>T	ENSP00000481063.1:p.Pro825Leu
ENST00000612417.4:c.1853+3215C>T	ENSP00000478360.1:n.1853+3215C>T
ENST00000621016.4:c.1866-4434C>T	ENSP00000480664.1:n.1866-4434C>T
NM_004360.3:c.2411C>T , LRG_301t1:c.2411C>T	NP_004351.1:p.Pro804Leu
XM_011523488.1:c.1676C>T	XP_011521790.1:p.Pro559Leu
XM_011523489.1:c.1676C>T	XP_011521791.1:p.Pro559Leu
NM_001317184.1:c.2228C>T	NP_001304113.1:p.Pro743Leu
NM_001317185.1:c.863C>T	NP_001304114.1:p.Pro288Leu
NM_001317186.1:c.446C>T	NP_001304115.1:p.Pro149Leu
NM_004360.4:c.2411C>T	NP_004351.1:p.Pro804Leu
NM_004360.5:c.2411C>T MANE Select	NP_004351.1:p.Pro804Leu
NM_001317184.2:c.2228C>T	NP_001304113.1:p.Pro743Leu
NM_001317185.2:c.863C>T	NP_001304114.1:p.Pro288Leu
NM_001317186.2:c.446C>T	NP_001304115.1:p.Pro149Leu