Canonical Allele Identifier: CA496393042

Gene: CDH1

Linked Data

• MyVariant Identifiers: chr16:g.68857318T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68823415T>A , CM000678.2:g.68823415T>A	GRCh38
NC_000016.9:g.68857318T>A , CM000678.1:g.68857318T>A	GRCh37
NC_000016.8:g.67414819T>A	NCBI36
NG_008021.1:g.91124T>A , LRG_301:g.91124T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261769.10:c.1953T>A MANE Select	ENSP00000261769.4:p.Ile651=
ENST00000261769.9:c.1953T>A	ENSP00000261769.4:p.Ile651=
ENST00000422392.6:c.1770T>A	ENSP00000414946.2:p.Ile590=
ENST00000562118.1:n.171T>A
ENST00000562836.5:n.2024T>A
ENST00000566510.5:c.*619T>A	ENSP00000458139.1:n.*619T>A
ENST00000566612.5:c.*193T>A	ENSP00000454782.1:n.*193T>A
ENST00000611625.4:c.2016T>A	ENSP00000481063.1:p.Ile672=
ENST00000612417.4:c.1830+1296T>A	ENSP00000478360.1:n.1830+1296T>A
ENST00000621016.4:c.1865+1261T>A	ENSP00000480664.1:n.1865+1261T>A
NM_004360.3:c.1953T>A , LRG_301t1:c.1953T>A	NP_004351.1:p.Ile651=
XM_011523488.1:c.1218T>A	XP_011521790.1:p.Ile406=
XM_011523489.1:c.1218T>A	XP_011521791.1:p.Ile406=
NM_001317184.1:c.1770T>A	NP_001304113.1:p.Ile590=
NM_001317185.1:c.405T>A	NP_001304114.1:p.Ile135=
NM_001317186.1:c.-13T>A	NP_001304115.1:n.-13T>A
NM_004360.4:c.1953T>A	NP_004351.1:p.Ile651=
NM_004360.5:c.1953T>A MANE Select	NP_004351.1:p.Ile651=
NM_001317184.2:c.1770T>A	NP_001304113.1:p.Ile590=
NM_001317185.2:c.405T>A	NP_001304114.1:p.Ile135=
NM_001317186.2:c.-13T>A	NP_001304115.1:n.-13T>A