Canonical Allele Identifier: CA2229915161

Gene: CDH1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68737424T= , CM000678.2:g.68737424T=	GRCh38
NC_000016.9:g.68771327T= , CM000678.1:g.68771327T=	GRCh37
NC_000016.8:g.67328828T=	NCBI36
NG_008021.1:g.5133T= , LRG_301:g.5133T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261769.10:c.9T= MANE Select	ENSP00000261769.4:p.Pro3=
ENST00000261769.9:c.9T=	ENSP00000261769.4:p.Pro3=
ENST00000422392.6:c.9T=	ENSP00000414946.2:p.Pro3=
ENST00000566510.5:c.9T=	ENSP00000458139.1:p.Pro3=
ENST00000566612.5:c.9T=	ENSP00000454782.1:p.Pro3=
ENST00000611625.4:c.9T=	ENSP00000481063.1:p.Pro3=
ENST00000612417.4:c.9T=	ENSP00000478360.1:p.Pro3=
ENST00000621016.4:c.9T=	ENSP00000480664.1:p.Pro3=
NM_004360.3:c.9T= , LRG_301t1:c.9T=	NP_004351.1:p.Pro3=
NM_001317184.1:c.9T=	NP_001304113.1:p.Pro3=
NM_001317185.1:c.-1607T=	NP_001304114.1:n.-1607T=
NM_001317186.1:c.-1811T=	NP_001304115.1:n.-1811T=
NM_004360.4:c.9T=	NP_004351.1:p.Pro3=
NM_004360.5:c.9T= MANE Select	NP_004351.1:p.Pro3=
NM_001317184.2:c.9T=	NP_001304113.1:p.Pro3=
NM_001317185.2:c.-1607T=	NP_001304114.1:n.-1607T=
NM_001317186.2:c.-1811T=	NP_001304115.1:n.-1811T=