Canonical Allele Identifier: CA2229983052

Gene: CDH1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68823514C= , CM000678.2:g.68823514C=	GRCh38
NC_000016.9:g.68857417C= , CM000678.1:g.68857417C=	GRCh37
NC_000016.8:g.67414918C=	NCBI36
NG_008021.1:g.91223C= , LRG_301:g.91223C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261769.10:c.2052C= MANE Select	ENSP00000261769.4:p.Ser684=
ENST00000261769.9:c.2052C=	ENSP00000261769.4:p.Ser684=
ENST00000422392.6:c.1869C=	ENSP00000414946.2:p.Ser623=
ENST00000562118.1:n.270C=
ENST00000562836.5:n.2123C=
ENST00000566510.5:c.*718C=	ENSP00000458139.1:n.*718C=
ENST00000566612.5:c.*292C=	ENSP00000454782.1:n.*292C=
ENST00000611625.4:c.2115C=	ENSP00000481063.1:p.Ser705=
ENST00000612417.4:c.1830+1395C=	ENSP00000478360.1:n.1830+1395C=
ENST00000621016.4:c.1865+1360C=	ENSP00000480664.1:n.1865+1360C=
NM_004360.3:c.2052C= , LRG_301t1:c.2052C=	NP_004351.1:p.Ser684=
XM_011523488.1:c.1317C=	XP_011521790.1:p.Ser439=
XM_011523489.1:c.1317C=	XP_011521791.1:p.Ser439=
NM_001317184.1:c.1869C=	NP_001304113.1:p.Ser623=
NM_001317185.1:c.504C=	NP_001304114.1:p.Ser168=
NM_001317186.1:c.87C=	NP_001304115.1:p.Ser29=
NM_004360.4:c.2052C=	NP_004351.1:p.Ser684=
NM_004360.5:c.2052C= MANE Select	NP_004351.1:p.Ser684=
NM_001317184.2:c.1869C=	NP_001304113.1:p.Ser623=
NM_001317185.2:c.504C=	NP_001304114.1:p.Ser168=
NM_001317186.2:c.87C=	NP_001304115.1:p.Ser29=