Canonical Allele Identifier: CA396472832

Gene: CDH1

Linked Data

• dbSNP Id: rs2152144220
• MyVariant Identifiers: chr16:g.68867379T>G (hg19) ; chr16:g.68833476T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68833476T>G , CM000678.2:g.68833476T>G	GRCh38
NC_000016.9:g.68867379T>G , CM000678.1:g.68867379T>G	GRCh37
NC_000016.8:g.67424880T>G	NCBI36
NG_008021.1:g.101185T>G , LRG_301:g.101185T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261769.10:c.2626T>G MANE Select	ENSP00000261769.4:p.Tyr876Asp
ENST00000261769.9:c.2626T>G	ENSP00000261769.4:p.Tyr876Asp
ENST00000422392.6:c.2443T>G	ENSP00000414946.2:p.Tyr815Asp
ENST00000562118.1:n.844T>G
ENST00000562836.5:n.2697T>G
ENST00000566510.5:c.*1292T>G	ENSP00000458139.1:n.*1292T>G
ENST00000566612.5:c.*866T>G	ENSP00000454782.1:n.*866T>G
ENST00000611625.4:c.2689T>G	ENSP00000481063.1:p.Tyr897Asp
ENST00000612417.4:c.1854-715T>G	ENSP00000478360.1:n.1854-715T>G
ENST00000621016.4:c.1866-727T>G	ENSP00000480664.1:n.1866-727T>G
NM_004360.3:c.2626T>G , LRG_301t1:c.2626T>G	NP_004351.1:p.Tyr876Asp
XM_011523488.1:c.1891T>G	XP_011521790.1:p.Tyr631Asp
XM_011523489.1:c.1891T>G	XP_011521791.1:p.Tyr631Asp
NM_001317184.1:c.2443T>G	NP_001304113.1:p.Tyr815Asp
NM_001317185.1:c.1078T>G	NP_001304114.1:p.Tyr360Asp
NM_001317186.1:c.661T>G	NP_001304115.1:p.Tyr221Asp
NM_004360.4:c.2626T>G	NP_004351.1:p.Tyr876Asp
NM_004360.5:c.2626T>G MANE Select	NP_004351.1:p.Tyr876Asp
NM_001317184.2:c.2443T>G	NP_001304113.1:p.Tyr815Asp
NM_001317185.2:c.1078T>G	NP_001304114.1:p.Tyr360Asp
NM_001317186.2:c.661T>G	NP_001304115.1:p.Tyr221Asp