Canonical Allele Identifier: CA496393013

Gene: CDH1

Linked Data

• dbSNP Id: rs1356090054
• MyVariant Identifiers: chr16:g.68857303C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68823400C>T , CM000678.2:g.68823400C>T	GRCh38
NC_000016.9:g.68857303C>T , CM000678.1:g.68857303C>T	GRCh37
NC_000016.8:g.67414804C>T	NCBI36
NG_008021.1:g.91109C>T , LRG_301:g.91109C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261769.10:c.1938C>T MANE Select	ENSP00000261769.4:p.Thr646=
ENST00000261769.9:c.1938C>T	ENSP00000261769.4:p.Thr646=
ENST00000422392.6:c.1755C>T	ENSP00000414946.2:p.Thr585=
ENST00000562118.1:n.156C>T
ENST00000562836.5:n.2009C>T
ENST00000566510.5:c.*604C>T	ENSP00000458139.1:n.*604C>T
ENST00000566612.5:c.*178C>T	ENSP00000454782.1:n.*178C>T
ENST00000611625.4:c.2001C>T	ENSP00000481063.1:p.Thr667=
ENST00000612417.4:c.1830+1281C>T	ENSP00000478360.1:n.1830+1281C>T
ENST00000621016.4:c.1865+1246C>T	ENSP00000480664.1:n.1865+1246C>T
NM_004360.3:c.1938C>T , LRG_301t1:c.1938C>T	NP_004351.1:p.Thr646=
XM_011523488.1:c.1203C>T	XP_011521790.1:p.Thr401=
XM_011523489.1:c.1203C>T	XP_011521791.1:p.Thr401=
NM_001317184.1:c.1755C>T	NP_001304113.1:p.Thr585=
NM_001317185.1:c.390C>T	NP_001304114.1:p.Thr130=
NM_001317186.1:c.-28C>T	NP_001304115.1:n.-28C>T
NM_004360.4:c.1938C>T	NP_004351.1:p.Thr646=
NM_004360.5:c.1938C>T MANE Select	NP_004351.1:p.Thr646=
NM_001317184.2:c.1755C>T	NP_001304113.1:p.Thr585=
NM_001317185.2:c.390C>T	NP_001304114.1:p.Thr130=
NM_001317186.2:c.-28C>T	NP_001304115.1:n.-28C>T