Canonical Allele Identifier: CA2229948601

Gene: CDH1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68815597C= , CM000678.2:g.68815597C=	GRCh38
NC_000016.9:g.68849500C= , CM000678.1:g.68849500C=	GRCh37
NC_000016.8:g.67407001C=	NCBI36
NG_008021.1:g.83306C= , LRG_301:g.83306C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000261769.10:c.1403C= MANE Select	ENSP00000261769.4:p.Thr468=
ENST00000261769.9:c.1403C=	ENSP00000261769.4:p.Thr468=
ENST00000422392.6:c.1220C=	ENSP00000414946.2:p.Thr407=
ENST00000562836.5:n.1474C=
ENST00000566510.5:c.*69C=	ENSP00000458139.1:n.*69C=
ENST00000566612.5:c.1403C=	ENSP00000454782.1:p.Thr468=
ENST00000611625.4:c.1466C=	ENSP00000481063.1:p.Thr489=
ENST00000612417.4:c.1403C=	ENSP00000478360.1:p.Thr468=
ENST00000621016.4:c.1403C=	ENSP00000480664.1:p.Thr468=
NM_004360.3:c.1403C= , LRG_301t1:c.1403C=	NP_004351.1:p.Thr468=
XM_011523488.1:c.668C=	XP_011521790.1:p.Thr223=
XM_011523489.1:c.668C=	XP_011521791.1:p.Thr223=
NM_001317184.1:c.1220C=	NP_001304113.1:p.Thr407=
NM_001317185.1:c.-146C=	NP_001304114.1:n.-146C=
NM_001317186.1:c.-417C=	NP_001304115.1:n.-417C=
NM_004360.4:c.1403C=	NP_004351.1:p.Thr468=
NM_004360.5:c.1403C= MANE Select	NP_004351.1:p.Thr468=
NM_001317184.2:c.1220C=	NP_001304113.1:p.Thr407=
NM_001317185.2:c.-146C=	NP_001304114.1:n.-146C=
NM_001317186.2:c.-417C=	NP_001304115.1:n.-417C=