Canonical Allele Identifier: CA2229991788

Gene: CDH1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68829576T= , CM000678.2:g.68829576T=	GRCh38
NC_000016.9:g.68863479T= , CM000678.1:g.68863479T=	GRCh37
NC_000016.8:g.67420980T=	NCBI36
NG_008021.1:g.97285T= , LRG_301:g.97285T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000261769.10:c.2296-78T= MANE Select	ENSP00000261769.4:n.2296-78T=
ENST00000261769.9:c.2296-78T=	ENSP00000261769.4:n.2296-78T=
ENST00000422392.6:c.2113-78T=	ENSP00000414946.2:n.2113-78T=
ENST00000562118.1:n.514-78T=
ENST00000562836.5:n.2367-78T=
ENST00000566510.5:c.*962-78T=	ENSP00000458139.1:n.*962-78T=
ENST00000566612.5:c.*536-78T=	ENSP00000454782.1:n.*536-78T=
ENST00000611625.4:c.2359-78T=	ENSP00000481063.1:n.2359-78T=
ENST00000612417.4:c.1853+3022T=	ENSP00000478360.1:n.1853+3022T=
ENST00000621016.4:c.1866-4627T=	ENSP00000480664.1:n.1866-4627T=
NM_004360.3:c.2296-78T= , LRG_301t1:c.2296-78T=	NP_004351.1:n.2296-78T=
XM_011523488.1:c.1561-78T=	XP_011521790.1:n.1561-78T=
XM_011523489.1:c.1561-78T=	XP_011521791.1:n.1561-78T=
NM_001317184.1:c.2113-78T=	NP_001304113.1:n.2113-78T=
NM_001317185.1:c.748-78T=	NP_001304114.1:n.748-78T=
NM_001317186.1:c.331-78T=	NP_001304115.1:n.331-78T=
NM_004360.4:c.2296-78T=	NP_004351.1:n.2296-78T=
NM_004360.5:c.2296-78T= MANE Select	NP_004351.1:n.2296-78T=
NM_001317184.2:c.2113-78T=	NP_001304113.1:n.2113-78T=
NM_001317185.2:c.748-78T=	NP_001304114.1:n.748-78T=
NM_001317186.2:c.331-78T=	NP_001304115.1:n.331-78T=