Canonical Allele Identifier: CA2229982643

Gene: CDH1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68823428A= , CM000678.2:g.68823428A=	GRCh38
NC_000016.9:g.68857331A= , CM000678.1:g.68857331A=	GRCh37
NC_000016.8:g.67414832A=	NCBI36
NG_008021.1:g.91137A= , LRG_301:g.91137A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261769.10:c.1966A= MANE Select	ENSP00000261769.4:p.Met656=
ENST00000261769.9:c.1966A=	ENSP00000261769.4:p.Met656=
ENST00000422392.6:c.1783A=	ENSP00000414946.2:p.Met595=
ENST00000562118.1:n.184A=
ENST00000562836.5:n.2037A=
ENST00000566510.5:c.*632A=	ENSP00000458139.1:n.*632A=
ENST00000566612.5:c.*206A=	ENSP00000454782.1:n.*206A=
ENST00000611625.4:c.2029A=	ENSP00000481063.1:p.Met677=
ENST00000612417.4:c.1830+1309A=	ENSP00000478360.1:n.1830+1309A=
ENST00000621016.4:c.1865+1274A=	ENSP00000480664.1:n.1865+1274A=
NM_004360.3:c.1966A= , LRG_301t1:c.1966A=	NP_004351.1:p.Met656=
XM_011523488.1:c.1231A=	XP_011521790.1:p.Met411=
XM_011523489.1:c.1231A=	XP_011521791.1:p.Met411=
NM_001317184.1:c.1783A=	NP_001304113.1:p.Met595=
NM_001317185.1:c.418A=	NP_001304114.1:p.Met140=
NM_001317186.1:c.1A=	NP_001304115.1:p.Met1=
NM_004360.4:c.1966A=	NP_004351.1:p.Met656=
NM_004360.5:c.1966A= MANE Select	NP_004351.1:p.Met656=
NM_001317184.2:c.1783A=	NP_001304113.1:p.Met595=
NM_001317185.2:c.418A=	NP_001304114.1:p.Met140=
NM_001317186.2:c.1A=	NP_001304115.1:p.Met1=