Canonical Allele Identifier: CA2229982628

Gene: CDH1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68823421G= , CM000678.2:g.68823421G=	GRCh38
NC_000016.9:g.68857324G= , CM000678.1:g.68857324G=	GRCh37
NC_000016.8:g.67414825G=	NCBI36
NG_008021.1:g.91130G= , LRG_301:g.91130G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261769.10:c.1959G= MANE Select	ENSP00000261769.4:p.Lys653=
ENST00000261769.9:c.1959G=	ENSP00000261769.4:p.Lys653=
ENST00000422392.6:c.1776G=	ENSP00000414946.2:p.Lys592=
ENST00000562118.1:n.177G=
ENST00000562836.5:n.2030G=
ENST00000566510.5:c.*625G=	ENSP00000458139.1:n.*625G=
ENST00000566612.5:c.*199G=	ENSP00000454782.1:n.*199G=
ENST00000611625.4:c.2022G=	ENSP00000481063.1:p.Lys674=
ENST00000612417.4:c.1830+1302G=	ENSP00000478360.1:n.1830+1302G=
ENST00000621016.4:c.1865+1267G=	ENSP00000480664.1:n.1865+1267G=
NM_004360.3:c.1959G= , LRG_301t1:c.1959G=	NP_004351.1:p.Lys653=
XM_011523488.1:c.1224G=	XP_011521790.1:p.Lys408=
XM_011523489.1:c.1224G=	XP_011521791.1:p.Lys408=
NM_001317184.1:c.1776G=	NP_001304113.1:p.Lys592=
NM_001317185.1:c.411G=	NP_001304114.1:p.Lys137=
NM_001317186.1:c.-7G=	NP_001304115.1:n.-7G=
NM_004360.4:c.1959G=	NP_004351.1:p.Lys653=
NM_004360.5:c.1959G= MANE Select	NP_004351.1:p.Lys653=
NM_001317184.2:c.1776G=	NP_001304113.1:p.Lys592=
NM_001317185.2:c.411G=	NP_001304114.1:p.Lys137=
NM_001317186.2:c.-7G=	NP_001304115.1:n.-7G=