Canonical Allele Identifier: CA2229977975

Gene: CDH1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68833102A= , CM000678.2:g.68833102A=	GRCh38
NC_000016.9:g.68867005A= , CM000678.1:g.68867005A=	GRCh37
NC_000016.8:g.67424506A=	NCBI36
NG_008021.1:g.100811A= , LRG_301:g.100811A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261769.10:c.2440-188A= MANE Select	ENSP00000261769.4:n.2440-188A=
ENST00000261769.9:c.2440-188A=	ENSP00000261769.4:n.2440-188A=
ENST00000422392.6:c.2257-188A=	ENSP00000414946.2:n.2257-188A=
ENST00000562118.1:n.658-188A=
ENST00000562836.5:n.2511-188A=
ENST00000566510.5:c.*1106-188A=	ENSP00000458139.1:n.*1106-188A=
ENST00000566612.5:c.*680-188A=	ENSP00000454782.1:n.*680-188A=
ENST00000611625.4:c.2503-188A=	ENSP00000481063.1:n.2503-188A=
ENST00000612417.4:c.1854-1089A=	ENSP00000478360.1:n.1854-1089A=
ENST00000621016.4:c.1866-1101A=	ENSP00000480664.1:n.1866-1101A=
NM_004360.3:c.2440-188A= , LRG_301t1:c.2440-188A=	NP_004351.1:n.2440-188A=
XM_011523488.1:c.1705-188A=	XP_011521790.1:n.1705-188A=
XM_011523489.1:c.1705-188A=	XP_011521791.1:n.1705-188A=
NM_001317184.1:c.2257-188A=	NP_001304113.1:n.2257-188A=
NM_001317185.1:c.892-188A=	NP_001304114.1:n.892-188A=
NM_001317186.1:c.475-188A=	NP_001304115.1:n.475-188A=
NM_004360.4:c.2440-188A=	NP_004351.1:n.2440-188A=
NM_004360.5:c.2440-188A= MANE Select	NP_004351.1:n.2440-188A=
NM_001317184.2:c.2257-188A=	NP_001304113.1:n.2257-188A=
NM_001317185.2:c.892-188A=	NP_001304114.1:n.892-188A=
NM_001317186.2:c.475-188A=	NP_001304115.1:n.475-188A=