Canonical Allele Identifier: CA2229992178

Gene: CDH1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68829691C= , CM000678.2:g.68829691C=	GRCh38
NC_000016.9:g.68863594C= , CM000678.1:g.68863594C=	GRCh37
NC_000016.8:g.67421095C=	NCBI36
NG_008021.1:g.97400C= , LRG_301:g.97400C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000261769.10:c.2333C= MANE Select	ENSP00000261769.4:p.Ala778=
ENST00000261769.9:c.2333C=	ENSP00000261769.4:p.Ala778=
ENST00000422392.6:c.2150C=	ENSP00000414946.2:p.Ala717=
ENST00000562118.1:n.551C=
ENST00000562836.5:n.2404C=
ENST00000566510.5:c.*999C=	ENSP00000458139.1:n.*999C=
ENST00000566612.5:c.*573C=	ENSP00000454782.1:n.*573C=
ENST00000611625.4:c.2396C=	ENSP00000481063.1:p.Ala799=
ENST00000612417.4:c.1853+3137C=	ENSP00000478360.1:n.1853+3137C=
ENST00000621016.4:c.1866-4512C=	ENSP00000480664.1:n.1866-4512C=
NM_004360.3:c.2333C= , LRG_301t1:c.2333C=	NP_004351.1:p.Ala778=
XM_011523488.1:c.1598C=	XP_011521790.1:p.Ala533=
XM_011523489.1:c.1598C=	XP_011521791.1:p.Ala533=
NM_001317184.1:c.2150C=	NP_001304113.1:p.Ala717=
NM_001317185.1:c.785C=	NP_001304114.1:p.Ala262=
NM_001317186.1:c.368C=	NP_001304115.1:p.Ala123=
NM_004360.4:c.2333C=	NP_004351.1:p.Ala778=
NM_004360.5:c.2333C= MANE Select	NP_004351.1:p.Ala778=
NM_001317184.2:c.2150C=	NP_001304113.1:p.Ala717=
NM_001317185.2:c.785C=	NP_001304114.1:p.Ala262=
NM_001317186.2:c.368C=	NP_001304115.1:p.Ala123=