Canonical Allele Identifier: CA2229978530

Gene: CDH1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68820026C= , CM000678.2:g.68820026C=	GRCh38
NC_000016.9:g.68853929C= , CM000678.1:g.68853929C=	GRCh37
NC_000016.8:g.67411430C=	NCBI36
NG_008021.1:g.87735C= , LRG_301:g.87735C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261769.10:c.1711+601C= MANE Select	ENSP00000261769.4:n.1711+601C=
ENST00000261769.9:c.1711+601C=	ENSP00000261769.4:n.1711+601C=
ENST00000422392.6:c.1528+601C=	ENSP00000414946.2:n.1528+601C=
ENST00000562836.5:n.1782+601C=
ENST00000566510.5:c.*377+601C=	ENSP00000458139.1:n.*377+601C=
ENST00000566612.5:c.1566-1975C=	ENSP00000454782.1:n.1566-1975C=
ENST00000611625.4:c.1774+601C=	ENSP00000481063.1:n.1774+601C=
ENST00000612417.4:c.1711+601C=	ENSP00000478360.1:n.1711+601C=
ENST00000621016.4:c.1711+601C=	ENSP00000480664.1:n.1711+601C=
NM_004360.3:c.1711+601C= , LRG_301t1:c.1711+601C=	NP_004351.1:n.1711+601C=
XM_011523488.1:c.976+601C=	XP_011521790.1:n.976+601C=
XM_011523489.1:c.976+601C=	XP_011521791.1:n.976+601C=
NM_001317184.1:c.1528+601C=	NP_001304113.1:n.1528+601C=
NM_001317185.1:c.163+601C=	NP_001304114.1:n.163+601C=
NM_001317186.1:c.-254-1975C=	NP_001304115.1:n.-254-1975C=
NM_004360.4:c.1711+601C=	NP_004351.1:n.1711+601C=
NM_004360.5:c.1711+601C= MANE Select	NP_004351.1:n.1711+601C=
NM_001317184.2:c.1528+601C=	NP_001304113.1:n.1528+601C=
NM_001317185.2:c.163+601C=	NP_001304114.1:n.163+601C=
NM_001317186.2:c.-254-1975C=	NP_001304115.1:n.-254-1975C=