Canonical Allele Identifier: CA2229980228

Gene: CDH1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68822006C= , CM000678.2:g.68822006C=	GRCh38
NC_000016.9:g.68855909C= , CM000678.1:g.68855909C=	GRCh37
NC_000016.8:g.67413410C=	NCBI36
NG_008021.1:g.89715C= , LRG_301:g.89715C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261769.10:c.1717C= MANE Select	ENSP00000261769.4:p.Pro573=
ENST00000261769.9:c.1717C=	ENSP00000261769.4:p.Pro573=
ENST00000422392.6:c.1534C=	ENSP00000414946.2:p.Pro512=
ENST00000562836.5:n.1788C=
ENST00000566510.5:c.*383C=	ENSP00000458139.1:n.*383C=
ENST00000566612.5:c.1571C=	ENSP00000454782.1:p.Ser524=
ENST00000611625.4:c.1780C=	ENSP00000481063.1:p.Pro594=
ENST00000612417.4:c.1717C=	ENSP00000478360.1:p.Pro573=
ENST00000621016.4:c.1717C=	ENSP00000480664.1:p.Pro573=
NM_004360.3:c.1717C= , LRG_301t1:c.1717C=	NP_004351.1:p.Pro573=
XM_011523488.1:c.982C=	XP_011521790.1:p.Pro328=
XM_011523489.1:c.982C=	XP_011521791.1:p.Pro328=
NM_001317184.1:c.1534C=	NP_001304113.1:p.Pro512=
NM_001317185.1:c.169C=	NP_001304114.1:p.Pro57=
NM_001317186.1:c.-249C=	NP_001304115.1:n.-249C=
NM_004360.4:c.1717C=	NP_004351.1:p.Pro573=
NM_004360.5:c.1717C= MANE Select	NP_004351.1:p.Pro573=
NM_001317184.2:c.1534C=	NP_001304113.1:p.Pro512=
NM_001317185.2:c.169C=	NP_001304114.1:p.Pro57=
NM_001317186.2:c.-249C=	NP_001304115.1:n.-249C=