Canonical Allele Identifier: CA2229914832

Gene: CDH1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68737294T= , CM000678.2:g.68737294T=	GRCh38
NC_000016.9:g.68771197T= , CM000678.1:g.68771197T=	GRCh37
NC_000016.8:g.67328698T=	NCBI36
NG_008021.1:g.5003T= , LRG_301:g.5003T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000261769.10:c.-122T= MANE Select	ENSP00000261769.4:n.-122T=
ENST00000261769.9:c.-122T=	ENSP00000261769.4:n.-122T=
ENST00000611625.4:c.-122T=	ENSP00000481063.1:n.-122T=
ENST00000612417.4:c.-122T=	ENSP00000478360.1:n.-122T=
NM_004360.3:c.-122T= , LRG_301t1:c.-122T=	NP_004351.1:n.-122T=
NM_001317184.1:c.-122T=	NP_001304113.1:n.-122T=
NM_001317185.1:c.-1737T=	NP_001304114.1:n.-1737T=
NM_001317186.1:c.-1941T=	NP_001304115.1:n.-1941T=
NM_004360.4:c.-122T=	NP_004351.1:n.-122T=
NM_004360.5:c.-122T= MANE Select	NP_004351.1:n.-122T=
NM_001317184.2:c.-122T=	NP_001304113.1:n.-122T=
NM_001317185.2:c.-1737T=	NP_001304114.1:n.-1737T=
NM_001317186.2:c.-1941T=	NP_001304115.1:n.-1941T=