Canonical Allele Identifier: CA2229991999

Gene: CDH1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68829654G= , CM000678.2:g.68829654G=	GRCh38
NC_000016.9:g.68863557G= , CM000678.1:g.68863557G=	GRCh37
NC_000016.8:g.67421058G=	NCBI36
NG_008021.1:g.97363G= , LRG_301:g.97363G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000261769.10:c.2296G= MANE Select	ENSP00000261769.4:p.Asp766=
ENST00000261769.9:c.2296G=	ENSP00000261769.4:p.Asp766=
ENST00000422392.6:c.2113G=	ENSP00000414946.2:p.Asp705=
ENST00000562118.1:n.514G=
ENST00000562836.5:n.2367G=
ENST00000566510.5:c.*962G=	ENSP00000458139.1:n.*962G=
ENST00000566612.5:c.*536G=	ENSP00000454782.1:n.*536G=
ENST00000611625.4:c.2359G=	ENSP00000481063.1:p.Asp787=
ENST00000612417.4:c.1853+3100G=	ENSP00000478360.1:n.1853+3100G=
ENST00000621016.4:c.1866-4549G=	ENSP00000480664.1:n.1866-4549G=
NM_004360.3:c.2296G= , LRG_301t1:c.2296G=	NP_004351.1:p.Asp766=
XM_011523488.1:c.1561G=	XP_011521790.1:p.Asp521=
XM_011523489.1:c.1561G=	XP_011521791.1:p.Asp521=
NM_001317184.1:c.2113G=	NP_001304113.1:p.Asp705=
NM_001317185.1:c.748G=	NP_001304114.1:p.Asp250=
NM_001317186.1:c.331G=	NP_001304115.1:p.Asp111=
NM_004360.4:c.2296G=	NP_004351.1:p.Asp766=
NM_004360.5:c.2296G= MANE Select	NP_004351.1:p.Asp766=
NM_001317184.2:c.2113G=	NP_001304113.1:p.Asp705=
NM_001317185.2:c.748G=	NP_001304114.1:p.Asp250=
NM_001317186.2:c.331G=	NP_001304115.1:p.Asp111=