Canonical Allele Identifier: CA396467036

Gene: CDH1

Linked Data

• MyVariant Identifiers: chr16:g.68856048T>G (hg19) ; chr16:g.68822145T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68822145T>G , CM000678.2:g.68822145T>G	GRCh38
NC_000016.9:g.68856048T>G , CM000678.1:g.68856048T>G	GRCh37
NC_000016.8:g.67413549T>G	NCBI36
NG_008021.1:g.89854T>G , LRG_301:g.89854T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000261769.10:c.1856T>G MANE Select	ENSP00000261769.4:p.Leu619Arg
ENST00000261769.9:c.1856T>G	ENSP00000261769.4:p.Leu619Arg
ENST00000422392.6:c.1673T>G	ENSP00000414946.2:p.Leu558Arg
ENST00000562836.5:n.1927T>G
ENST00000566510.5:c.*522T>G	ENSP00000458139.1:n.*522T>G
ENST00000566612.5:c.*96T>G	ENSP00000454782.1:n.*96T>G
ENST00000611625.4:c.1919T>G	ENSP00000481063.1:p.Leu640Arg
ENST00000612417.4:c.1830+26T>G	ENSP00000478360.1:n.1830+26T>G
ENST00000621016.4:c.1856T>G	ENSP00000480664.1:p.Leu619Arg
NM_004360.3:c.1856T>G , LRG_301t1:c.1856T>G	NP_004351.1:p.Leu619Arg
XM_011523488.1:c.1121T>G	XP_011521790.1:p.Leu374Arg
XM_011523489.1:c.1121T>G	XP_011521791.1:p.Leu374Arg
NM_001317184.1:c.1673T>G	NP_001304113.1:p.Leu558Arg
NM_001317185.1:c.308T>G	NP_001304114.1:p.Leu103Arg
NM_001317186.1:c.-110T>G	NP_001304115.1:n.-110T>G
NM_004360.4:c.1856T>G	NP_004351.1:p.Leu619Arg
NM_004360.5:c.1856T>G MANE Select	NP_004351.1:p.Leu619Arg
NM_001317184.2:c.1673T>G	NP_001304113.1:p.Leu558Arg
NM_001317185.2:c.308T>G	NP_001304114.1:p.Leu103Arg
NM_001317186.2:c.-110T>G	NP_001304115.1:n.-110T>G