Canonical Allele Identifier: CA2229982213

Gene: CDH1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68823261T= , CM000678.2:g.68823261T=	GRCh38
NC_000016.9:g.68857164T= , CM000678.1:g.68857164T=	GRCh37
NC_000016.8:g.67414665T=	NCBI36
NG_008021.1:g.90970T= , LRG_301:g.90970T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261769.10:c.1937-138T= MANE Select	ENSP00000261769.4:n.1937-138T=
ENST00000261769.9:c.1937-138T=	ENSP00000261769.4:n.1937-138T=
ENST00000422392.6:c.1754-138T=	ENSP00000414946.2:n.1754-138T=
ENST00000562118.1:n.17T=
ENST00000562836.5:n.2008-138T=
ENST00000566510.5:c.*603-138T=	ENSP00000458139.1:n.*603-138T=
ENST00000566612.5:c.*177-138T=	ENSP00000454782.1:n.*177-138T=
ENST00000611625.4:c.2000-138T=	ENSP00000481063.1:n.2000-138T=
ENST00000612417.4:c.1830+1142T=	ENSP00000478360.1:n.1830+1142T=
ENST00000621016.4:c.1865+1107T=	ENSP00000480664.1:n.1865+1107T=
NM_004360.3:c.1937-138T= , LRG_301t1:c.1937-138T=	NP_004351.1:n.1937-138T=
XM_011523488.1:c.1202-138T=	XP_011521790.1:n.1202-138T=
XM_011523489.1:c.1202-138T=	XP_011521791.1:n.1202-138T=
NM_001317184.1:c.1754-138T=	NP_001304113.1:n.1754-138T=
NM_001317185.1:c.389-138T=	NP_001304114.1:n.389-138T=
NM_001317186.1:c.-29-138T=	NP_001304115.1:n.-29-138T=
NM_004360.4:c.1937-138T=	NP_004351.1:n.1937-138T=
NM_004360.5:c.1937-138T= MANE Select	NP_004351.1:n.1937-138T=
NM_001317184.2:c.1754-138T=	NP_001304113.1:n.1754-138T=
NM_001317185.2:c.389-138T=	NP_001304114.1:n.389-138T=
NM_001317186.2:c.-29-138T=	NP_001304115.1:n.-29-138T=