Canonical Allele Identifier: CA2229992150

Gene: CDH1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68829688A= , CM000678.2:g.68829688A=	GRCh38
NC_000016.9:g.68863591A= , CM000678.1:g.68863591A=	GRCh37
NC_000016.8:g.67421092A=	NCBI36
NG_008021.1:g.97397A= , LRG_301:g.97397A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000261769.10:c.2330A= MANE Select	ENSP00000261769.4:p.Asp777=
ENST00000261769.9:c.2330A=	ENSP00000261769.4:p.Asp777=
ENST00000422392.6:c.2147A=	ENSP00000414946.2:p.Asp716=
ENST00000562118.1:n.548A=
ENST00000562836.5:n.2401A=
ENST00000566510.5:c.*996A=	ENSP00000458139.1:n.*996A=
ENST00000566612.5:c.*570A=	ENSP00000454782.1:n.*570A=
ENST00000611625.4:c.2393A=	ENSP00000481063.1:p.Asp798=
ENST00000612417.4:c.1853+3134A=	ENSP00000478360.1:n.1853+3134A=
ENST00000621016.4:c.1866-4515A=	ENSP00000480664.1:n.1866-4515A=
NM_004360.3:c.2330A= , LRG_301t1:c.2330A=	NP_004351.1:p.Asp777=
XM_011523488.1:c.1595A=	XP_011521790.1:p.Asp532=
XM_011523489.1:c.1595A=	XP_011521791.1:p.Asp532=
NM_001317184.1:c.2147A=	NP_001304113.1:p.Asp716=
NM_001317185.1:c.782A=	NP_001304114.1:p.Asp261=
NM_001317186.1:c.365A=	NP_001304115.1:p.Asp122=
NM_004360.4:c.2330A=	NP_004351.1:p.Asp777=
NM_004360.5:c.2330A= MANE Select	NP_004351.1:p.Asp777=
NM_001317184.2:c.2147A=	NP_001304113.1:p.Asp716=
NM_001317185.2:c.782A=	NP_001304114.1:p.Asp261=
NM_001317186.2:c.365A=	NP_001304115.1:p.Asp122=