Canonical Allele Identifier: CA2229914880

Gene: CDH1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68737332G= , CM000678.2:g.68737332G=	GRCh38
NC_000016.9:g.68771235G= , CM000678.1:g.68771235G=	GRCh37
NC_000016.8:g.67328736G=	NCBI36
NG_008021.1:g.5041G= , LRG_301:g.5041G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261769.10:c.-84G= MANE Select	ENSP00000261769.4:n.-84G=
ENST00000261769.9:c.-84G=	ENSP00000261769.4:n.-84G=
ENST00000566612.5:c.-84G=	ENSP00000454782.1:n.-84G=
ENST00000611625.4:c.-84G=	ENSP00000481063.1:n.-84G=
ENST00000612417.4:c.-84G=	ENSP00000478360.1:n.-84G=
ENST00000621016.4:c.-84G=	ENSP00000480664.1:n.-84G=
NM_004360.3:c.-84G= , LRG_301t1:c.-84G=	NP_004351.1:n.-84G=
NM_001317184.1:c.-84G=	NP_001304113.1:n.-84G=
NM_001317185.1:c.-1699G=	NP_001304114.1:n.-1699G=
NM_001317186.1:c.-1903G=	NP_001304115.1:n.-1903G=
NM_004360.4:c.-84G=	NP_004351.1:n.-84G=
NM_004360.5:c.-84G= MANE Select	NP_004351.1:n.-84G=
NM_001317184.2:c.-84G=	NP_001304113.1:n.-84G=
NM_001317185.2:c.-1699G=	NP_001304114.1:n.-1699G=
NM_001317186.2:c.-1903G=	NP_001304115.1:n.-1903G=