Canonical Allele Identifier: CA2229992211

Gene: CDH1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68829697C= , CM000678.2:g.68829697C=	GRCh38
NC_000016.9:g.68863600C= , CM000678.1:g.68863600C=	GRCh37
NC_000016.8:g.67421101C=	NCBI36
NG_008021.1:g.97406C= , LRG_301:g.97406C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000261769.10:c.2339C= MANE Select	ENSP00000261769.4:p.Pro780=
ENST00000261769.9:c.2339C=	ENSP00000261769.4:p.Pro780=
ENST00000422392.6:c.2156C=	ENSP00000414946.2:p.Pro719=
ENST00000562118.1:n.557C=
ENST00000562836.5:n.2410C=
ENST00000566510.5:c.*1005C=	ENSP00000458139.1:n.*1005C=
ENST00000566612.5:c.*579C=	ENSP00000454782.1:n.*579C=
ENST00000611625.4:c.2402C=	ENSP00000481063.1:p.Pro801=
ENST00000612417.4:c.1853+3143C=	ENSP00000478360.1:n.1853+3143C=
ENST00000621016.4:c.1866-4506C=	ENSP00000480664.1:n.1866-4506C=
NM_004360.3:c.2339C= , LRG_301t1:c.2339C=	NP_004351.1:p.Pro780=
XM_011523488.1:c.1604C=	XP_011521790.1:p.Pro535=
XM_011523489.1:c.1604C=	XP_011521791.1:p.Pro535=
NM_001317184.1:c.2156C=	NP_001304113.1:p.Pro719=
NM_001317185.1:c.791C=	NP_001304114.1:p.Pro264=
NM_001317186.1:c.374C=	NP_001304115.1:p.Pro125=
NM_004360.4:c.2339C=	NP_004351.1:p.Pro780=
NM_004360.5:c.2339C= MANE Select	NP_004351.1:p.Pro780=
NM_001317184.2:c.2156C=	NP_001304113.1:p.Pro719=
NM_001317185.2:c.791C=	NP_001304114.1:p.Pro264=
NM_001317186.2:c.374C=	NP_001304115.1:p.Pro125=