Canonical Allele Identifier: CA2229974992

Gene: CDH1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68829733T= , CM000678.2:g.68829733T=	GRCh38
NC_000016.9:g.68863636T= , CM000678.1:g.68863636T=	GRCh37
NC_000016.8:g.67421137T=	NCBI36
NG_008021.1:g.97442T= , LRG_301:g.97442T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261769.10:c.2375T= MANE Select	ENSP00000261769.4:p.Met792=
ENST00000261769.9:c.2375T=	ENSP00000261769.4:p.Met792=
ENST00000422392.6:c.2192T=	ENSP00000414946.2:p.Met731=
ENST00000562118.1:n.593T=
ENST00000562836.5:n.2446T=
ENST00000566510.5:c.*1041T=	ENSP00000458139.1:n.*1041T=
ENST00000566612.5:c.*615T=	ENSP00000454782.1:n.*615T=
ENST00000611625.4:c.2438T=	ENSP00000481063.1:p.Met813=
ENST00000612417.4:c.1853+3179T=	ENSP00000478360.1:n.1853+3179T=
ENST00000621016.4:c.1866-4470T=	ENSP00000480664.1:n.1866-4470T=
NM_004360.3:c.2375T= , LRG_301t1:c.2375T=	NP_004351.1:p.Met792=
XM_011523488.1:c.1640T=	XP_011521790.1:p.Met547=
XM_011523489.1:c.1640T=	XP_011521791.1:p.Met547=
NM_001317184.1:c.2192T=	NP_001304113.1:p.Met731=
NM_001317185.1:c.827T=	NP_001304114.1:p.Met276=
NM_001317186.1:c.410T=	NP_001304115.1:p.Met137=
NM_004360.4:c.2375T=	NP_004351.1:p.Met792=
NM_004360.5:c.2375T= MANE Select	NP_004351.1:p.Met792=
NM_001317184.2:c.2192T=	NP_001304113.1:p.Met731=
NM_001317185.2:c.827T=	NP_001304114.1:p.Met276=
NM_001317186.2:c.410T=	NP_001304115.1:p.Met137=