Canonical Allele Identifier: CA283320271

Gene: CDH1

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68834619T>G , CM000678.2:g.68834619T>G	GRCh38
NC_000016.9:g.68868522T>G , CM000678.1:g.68868522T>G	GRCh37
NC_000016.8:g.67426023T>G	NCBI36
NG_008021.1:g.102328T>G , LRG_301:g.102328T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261769.10:c.*1120T>G MANE Select	ENSP00000261769.4:n.*1120T>G
ENST00000261769.9:c.*1120T>G	ENSP00000261769.4:n.*1120T>G
ENST00000566612.5:c.*2009T>G	ENSP00000454782.1:n.*2009T>G
ENST00000611625.4:c.*1120T>G	ENSP00000481063.1:n.*1120T>G
ENST00000621016.4:c.*338T>G	ENSP00000480664.1:n.*338T>G
NM_004360.3:c.*1120T>G , LRG_301t1:c.*1120T>G	NP_004351.1:n.*1120T>G
XM_011523488.1:c.*1120T>G	XP_011521790.1:n.*1120T>G
XM_011523489.1:c.*1120T>G	XP_011521791.1:n.*1120T>G
NM_001317184.1:c.*1120T>G	NP_001304113.1:n.*1120T>G
NM_001317185.1:c.*1120T>G	NP_001304114.1:n.*1120T>G
NM_001317186.1:c.*1120T>G	NP_001304115.1:n.*1120T>G
NM_004360.4:c.*1120T>G	NP_004351.1:n.*1120T>G
NM_004360.5:c.*1120T>G MANE Select	NP_004351.1:n.*1120T>G
NM_001317184.2:c.*1120T>G	NP_001304113.1:n.*1120T>G
NM_001317185.2:c.*1120T>G	NP_001304114.1:n.*1120T>G
NM_001317186.2:c.*1120T>G	NP_001304115.1:n.*1120T>G