Canonical Allele Identifier: CA396467097

Gene: CDH1

Linked Data

• dbSNP Id: rs1555516877
• MyVariant Identifiers: chr16:g.68856065C>A (hg19) ; chr16:g.68822162C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68822162C>A , CM000678.2:g.68822162C>A	GRCh38
NC_000016.9:g.68856065C>A , CM000678.1:g.68856065C>A	GRCh37
NC_000016.8:g.67413566C>A	NCBI36
NG_008021.1:g.89871C>A , LRG_301:g.89871C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261769.10:c.1873C>A MANE Select	ENSP00000261769.4:p.Pro625Thr
ENST00000261769.9:c.1873C>A	ENSP00000261769.4:p.Pro625Thr
ENST00000422392.6:c.1690C>A	ENSP00000414946.2:p.Pro564Thr
ENST00000562836.5:n.1944C>A
ENST00000566510.5:c.*539C>A	ENSP00000458139.1:n.*539C>A
ENST00000566612.5:c.*113C>A	ENSP00000454782.1:n.*113C>A
ENST00000611625.4:c.1936C>A	ENSP00000481063.1:p.Pro646Thr
ENST00000612417.4:c.1830+43C>A	ENSP00000478360.1:n.1830+43C>A
ENST00000621016.4:c.1865+8C>A	ENSP00000480664.1:n.1865+8C>A
NM_004360.3:c.1873C>A , LRG_301t1:c.1873C>A	NP_004351.1:p.Pro625Thr
XM_011523488.1:c.1138C>A	XP_011521790.1:p.Pro380Thr
XM_011523489.1:c.1138C>A	XP_011521791.1:p.Pro380Thr
NM_001317184.1:c.1690C>A	NP_001304113.1:p.Pro564Thr
NM_001317185.1:c.325C>A	NP_001304114.1:p.Pro109Thr
NM_001317186.1:c.-93C>A	NP_001304115.1:n.-93C>A
NM_004360.4:c.1873C>A	NP_004351.1:p.Pro625Thr
NM_004360.5:c.1873C>A MANE Select	NP_004351.1:p.Pro625Thr
NM_001317184.2:c.1690C>A	NP_001304113.1:p.Pro564Thr
NM_001317185.2:c.325C>A	NP_001304114.1:p.Pro109Thr
NM_001317186.2:c.-93C>A	NP_001304115.1:n.-93C>A