Canonical Allele Identifier: CA2229916405

Gene: CDH1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68738303T= , CM000678.2:g.68738303T=	GRCh38
NC_000016.9:g.68772206T= , CM000678.1:g.68772206T=	GRCh37
NC_000016.8:g.67329707T=	NCBI36
NG_008021.1:g.6012T= , LRG_301:g.6012T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000261769.10:c.55T= MANE Select	ENSP00000261769.4:p.Ser19=
ENST00000261769.9:c.55T=	ENSP00000261769.4:p.Ser19=
ENST00000422392.6:c.55T=	ENSP00000414946.2:p.Ser19=
ENST00000566510.5:c.55T=	ENSP00000458139.1:p.Ser19=
ENST00000566612.5:c.55T=	ENSP00000454782.1:p.Ser19=
ENST00000611625.4:c.55T=	ENSP00000481063.1:p.Ser19=
ENST00000612417.4:c.55T=	ENSP00000478360.1:p.Ser19=
ENST00000621016.4:c.55T=	ENSP00000480664.1:p.Ser19=
NM_004360.3:c.55T= , LRG_301t1:c.55T=	NP_004351.1:p.Ser19=
NM_001317184.1:c.55T=	NP_001304113.1:p.Ser19=
NM_001317185.1:c.-1561T=	NP_001304114.1:n.-1561T=
NM_001317186.1:c.-1765T=	NP_001304115.1:n.-1765T=
NM_004360.4:c.55T=	NP_004351.1:p.Ser19=
NM_004360.5:c.55T= MANE Select	NP_004351.1:p.Ser19=
NM_001317184.2:c.55T=	NP_001304113.1:p.Ser19=
NM_001317185.2:c.-1561T=	NP_001304114.1:n.-1561T=
NM_001317186.2:c.-1765T=	NP_001304115.1:n.-1765T=