Canonical Allele Identifier: CA2229979807

Gene: CDH1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68834546G= , CM000678.2:g.68834546G=	GRCh38
NC_000016.9:g.68868449G= , CM000678.1:g.68868449G=	GRCh37
NC_000016.8:g.67425950G=	NCBI36
NG_008021.1:g.102255G= , LRG_301:g.102255G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000261769.10:c.*1047G= MANE Select	ENSP00000261769.4:n.*1047G=
ENST00000261769.9:c.*1047G=	ENSP00000261769.4:n.*1047G=
ENST00000566612.5:c.*1936G=	ENSP00000454782.1:n.*1936G=
ENST00000611625.4:c.*1047G=	ENSP00000481063.1:n.*1047G=
ENST00000621016.4:c.*265G=	ENSP00000480664.1:n.*265G=
NM_004360.3:c.*1047G= , LRG_301t1:c.*1047G=	NP_004351.1:n.*1047G=
XM_011523488.1:c.*1047G=	XP_011521790.1:n.*1047G=
XM_011523489.1:c.*1047G=	XP_011521791.1:n.*1047G=
NM_001317184.1:c.*1047G=	NP_001304113.1:n.*1047G=
NM_001317185.1:c.*1047G=	NP_001304114.1:n.*1047G=
NM_001317186.1:c.*1047G=	NP_001304115.1:n.*1047G=
NM_004360.4:c.*1047G=	NP_004351.1:n.*1047G=
NM_004360.5:c.*1047G= MANE Select	NP_004351.1:n.*1047G=
NM_001317184.2:c.*1047G=	NP_001304113.1:n.*1047G=
NM_001317185.2:c.*1047G=	NP_001304114.1:n.*1047G=
NM_001317186.2:c.*1047G=	NP_001304115.1:n.*1047G=