Canonical Allele Identifier: CA2229969987

Gene: CDH1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68812263G= , CM000678.2:g.68812263G=	GRCh38
NC_000016.9:g.68846166G= , CM000678.1:g.68846166G=	GRCh37
NC_000016.8:g.67403667G=	NCBI36
NG_008021.1:g.79972G= , LRG_301:g.79972G=

Transcript Alleles

HGVS	Amino-acid Change
NM_004360.5:c.1137G= MANE Select	NP_004351.1:p.Thr379=
ENST00000261769.10:c.1137G= MANE Select	ENSP00000261769.4:p.Thr379=
NM_001317184.1:c.1137G=	NP_001304113.1:p.Thr379=
NM_001317184.2:c.1137G=	NP_001304113.1:p.Thr379=
NM_001317185.1:c.-479G=	NP_001304114.1:n.-479G=
NM_001317185.2:c.-479G=	NP_001304114.1:n.-479G=
NM_001317186.1:c.-683G=	NP_001304115.1:n.-683G=
NM_001317186.2:c.-683G=	NP_001304115.1:n.-683G=
NM_004360.3:c.1137G= , LRG_301t1:c.1137G=	NP_004351.1:p.Thr379=
NM_004360.4:c.1137G=	NP_004351.1:p.Thr379=
ENST00000261769.9:c.1137G=	ENSP00000261769.4:p.Thr379=
ENST00000422392.6:c.1137G=	ENSP00000414946.2:p.Thr379=
ENST00000562836.5:n.1208G=
ENST00000565810.1:n.181G=
ENST00000566510.5:c.981G=	ENSP00000458139.1:p.Thr327=
ENST00000566612.5:c.1137G=	ENSP00000454782.1:p.Thr379=
ENST00000611625.4:c.1137G=	ENSP00000481063.1:p.Thr379=
ENST00000612417.4:c.1137G=	ENSP00000478360.1:p.Thr379=
ENST00000621016.4:c.1137G=	ENSP00000480664.1:p.Thr379=
XM_011523488.1:c.402G=	XP_011521790.1:p.Thr134=
XM_011523489.1:c.402G=	XP_011521791.1:p.Thr134=