Canonical Allele Identifier: CA8129996

Gene: CDH1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68812229C>G , CM000678.2:g.68812229C>G	GRCh38
NC_000016.9:g.68846132C>G , CM000678.1:g.68846132C>G	GRCh37
NC_000016.8:g.67403633C>G	NCBI36
NG_008021.1:g.79938C>G , LRG_301:g.79938C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_004360.5:c.1103C>G MANE Select	NP_004351.1:p.Thr368Ser
ENST00000261769.10:c.1103C>G MANE Select	ENSP00000261769.4:p.Thr368Ser
NM_001317184.1:c.1103C>G	NP_001304113.1:p.Thr368Ser
NM_001317184.2:c.1103C>G	NP_001304113.1:p.Thr368Ser
NM_001317185.1:c.-513C>G	NP_001304114.1:n.-513C>G
NM_001317185.2:c.-513C>G	NP_001304114.1:n.-513C>G
NM_001317186.1:c.-717C>G	NP_001304115.1:n.-717C>G
NM_001317186.2:c.-717C>G	NP_001304115.1:n.-717C>G
NM_004360.3:c.1103C>G , LRG_301t1:c.1103C>G	NP_004351.1:p.Thr368Ser
NM_004360.4:c.1103C>G	NP_004351.1:p.Thr368Ser
ENST00000261769.9:c.1103C>G	ENSP00000261769.4:p.Thr368Ser
ENST00000422392.6:c.1103C>G	ENSP00000414946.2:p.Thr368Ser
ENST00000561751.1:c.725C>G
ENST00000562836.5:n.1174C>G
ENST00000565810.1:n.147C>G
ENST00000566510.5:c.947C>G	ENSP00000458139.1:p.Thr316Ser
ENST00000566612.5:c.1103C>G	ENSP00000454782.1:p.Thr368Ser
ENST00000611625.4:c.1103C>G	ENSP00000481063.1:p.Thr368Ser
ENST00000612417.4:c.1103C>G	ENSP00000478360.1:p.Thr368Ser
ENST00000621016.4:c.1103C>G	ENSP00000480664.1:p.Thr368Ser
XM_011523488.1:c.368C>G	XP_011521790.1:p.Thr123Ser
XM_011523489.1:c.368C>G	XP_011521791.1:p.Thr123Ser