Canonical Allele Identifier: CA2229978194

Gene: CDH1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68833368T= , CM000678.2:g.68833368T=	GRCh38
NC_000016.9:g.68867271T= , CM000678.1:g.68867271T=	GRCh37
NC_000016.8:g.67424772T=	NCBI36
NG_008021.1:g.101077T= , LRG_301:g.101077T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261769.10:c.2518T= MANE Select	ENSP00000261769.4:p.Ser840=
ENST00000261769.9:c.2518T=	ENSP00000261769.4:p.Ser840=
ENST00000422392.6:c.2335T=	ENSP00000414946.2:p.Ser779=
ENST00000562118.1:n.736T=
ENST00000562836.5:n.2589T=
ENST00000566510.5:c.*1184T=	ENSP00000458139.1:n.*1184T=
ENST00000566612.5:c.*758T=	ENSP00000454782.1:n.*758T=
ENST00000611625.4:c.2581T=	ENSP00000481063.1:p.Ser861=
ENST00000612417.4:c.1854-823T=	ENSP00000478360.1:n.1854-823T=
ENST00000621016.4:c.1866-835T=	ENSP00000480664.1:n.1866-835T=
NM_004360.3:c.2518T= , LRG_301t1:c.2518T=	NP_004351.1:p.Ser840=
XM_011523488.1:c.1783T=	XP_011521790.1:p.Ser595=
XM_011523489.1:c.1783T=	XP_011521791.1:p.Ser595=
NM_001317184.1:c.2335T=	NP_001304113.1:p.Ser779=
NM_001317185.1:c.970T=	NP_001304114.1:p.Ser324=
NM_001317186.1:c.553T=	NP_001304115.1:p.Ser185=
NM_004360.4:c.2518T=	NP_004351.1:p.Ser840=
NM_004360.5:c.2518T= MANE Select	NP_004351.1:p.Ser840=
NM_001317184.2:c.2335T=	NP_001304113.1:p.Ser779=
NM_001317185.2:c.970T=	NP_001304114.1:p.Ser324=
NM_001317186.2:c.553T=	NP_001304115.1:p.Ser185=