Canonical Allele Identifier: CA283320232

Gene: CDH1

Linked Data

• dbSNP Id: rs1042494185
• gnomAD v3: 16-68834562-C-T
• gnomAD v4: 16-68834562-C-T
• MyVariant Identifiers: chr16:g.68868465C>T (hg19) ; chr16:g.68834562C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68834562C>T , CM000678.2:g.68834562C>T	GRCh38
NC_000016.9:g.68868465C>T , CM000678.1:g.68868465C>T	GRCh37
NC_000016.8:g.67425966C>T	NCBI36
NG_008021.1:g.102271C>T , LRG_301:g.102271C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000261769.10:c.*1063C>T MANE Select	ENSP00000261769.4:n.*1063C>T
ENST00000261769.9:c.*1063C>T	ENSP00000261769.4:n.*1063C>T
ENST00000566612.5:c.*1952C>T	ENSP00000454782.1:n.*1952C>T
ENST00000611625.4:c.*1063C>T	ENSP00000481063.1:n.*1063C>T
ENST00000621016.4:c.*281C>T	ENSP00000480664.1:n.*281C>T
NM_004360.3:c.*1063C>T , LRG_301t1:c.*1063C>T	NP_004351.1:n.*1063C>T
XM_011523488.1:c.*1063C>T	XP_011521790.1:n.*1063C>T
XM_011523489.1:c.*1063C>T	XP_011521791.1:n.*1063C>T
NM_001317184.1:c.*1063C>T	NP_001304113.1:n.*1063C>T
NM_001317185.1:c.*1063C>T	NP_001304114.1:n.*1063C>T
NM_001317186.1:c.*1063C>T	NP_001304115.1:n.*1063C>T
NM_004360.4:c.*1063C>T	NP_004351.1:n.*1063C>T
NM_004360.5:c.*1063C>T MANE Select	NP_004351.1:n.*1063C>T
NM_001317184.2:c.*1063C>T	NP_001304113.1:n.*1063C>T
NM_001317185.2:c.*1063C>T	NP_001304114.1:n.*1063C>T
NM_001317186.2:c.*1063C>T	NP_001304115.1:n.*1063C>T