Canonical Allele Identifier: CA2229980782

Gene: CDH1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68822158A= , CM000678.2:g.68822158A=	GRCh38
NC_000016.9:g.68856061A= , CM000678.1:g.68856061A=	GRCh37
NC_000016.8:g.67413562A=	NCBI36
NG_008021.1:g.89867A= , LRG_301:g.89867A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261769.10:c.1869A= MANE Select	ENSP00000261769.4:p.Thr623=
ENST00000261769.9:c.1869A=	ENSP00000261769.4:p.Thr623=
ENST00000422392.6:c.1686A=	ENSP00000414946.2:p.Thr562=
ENST00000562836.5:n.1940A=
ENST00000566510.5:c.*535A=	ENSP00000458139.1:n.*535A=
ENST00000566612.5:c.*109A=	ENSP00000454782.1:n.*109A=
ENST00000611625.4:c.1932A=	ENSP00000481063.1:p.Thr644=
ENST00000612417.4:c.1830+39A=	ENSP00000478360.1:n.1830+39A=
ENST00000621016.4:c.1865+4A=	ENSP00000480664.1:n.1865+4A=
NM_004360.3:c.1869A= , LRG_301t1:c.1869A=	NP_004351.1:p.Thr623=
XM_011523488.1:c.1134A=	XP_011521790.1:p.Thr378=
XM_011523489.1:c.1134A=	XP_011521791.1:p.Thr378=
NM_001317184.1:c.1686A=	NP_001304113.1:p.Thr562=
NM_001317185.1:c.321A=	NP_001304114.1:p.Thr107=
NM_001317186.1:c.-97A=	NP_001304115.1:n.-97A=
NM_004360.4:c.1869A=	NP_004351.1:p.Thr623=
NM_004360.5:c.1869A= MANE Select	NP_004351.1:p.Thr623=
NM_001317184.2:c.1686A=	NP_001304113.1:p.Thr562=
NM_001317185.2:c.321A=	NP_001304114.1:p.Thr107=
NM_001317186.2:c.-97A=	NP_001304115.1:n.-97A=