Canonical Allele Identifier: CA396472839

Gene: CDH1

Linked Data

• ClinVar Variation Id: 1715892
• ClinVar RCV Id: RCV002301589 ; RCV002427761
• dbSNP Id: rs2152144226
• MyVariant Identifiers: chr16:g.68867380A>T (hg19) ; chr16:g.68833477A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68833477A>T , CM000678.2:g.68833477A>T	GRCh38
NC_000016.9:g.68867380A>T , CM000678.1:g.68867380A>T	GRCh37
NC_000016.8:g.67424881A>T	NCBI36
NG_008021.1:g.101186A>T , LRG_301:g.101186A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261769.10:c.2627A>T MANE Select	ENSP00000261769.4:p.Tyr876Phe
ENST00000261769.9:c.2627A>T	ENSP00000261769.4:p.Tyr876Phe
ENST00000422392.6:c.2444A>T	ENSP00000414946.2:p.Tyr815Phe
ENST00000562118.1:n.845A>T
ENST00000562836.5:n.2698A>T
ENST00000566510.5:c.*1293A>T	ENSP00000458139.1:n.*1293A>T
ENST00000566612.5:c.*867A>T	ENSP00000454782.1:n.*867A>T
ENST00000611625.4:c.2690A>T	ENSP00000481063.1:p.Tyr897Phe
ENST00000612417.4:c.1854-714A>T	ENSP00000478360.1:n.1854-714A>T
ENST00000621016.4:c.1866-726A>T	ENSP00000480664.1:n.1866-726A>T
NM_004360.3:c.2627A>T , LRG_301t1:c.2627A>T	NP_004351.1:p.Tyr876Phe
XM_011523488.1:c.1892A>T	XP_011521790.1:p.Tyr631Phe
XM_011523489.1:c.1892A>T	XP_011521791.1:p.Tyr631Phe
NM_001317184.1:c.2444A>T	NP_001304113.1:p.Tyr815Phe
NM_001317185.1:c.1079A>T	NP_001304114.1:p.Tyr360Phe
NM_001317186.1:c.662A>T	NP_001304115.1:p.Tyr221Phe
NM_004360.4:c.2627A>T	NP_004351.1:p.Tyr876Phe
NM_004360.5:c.2627A>T MANE Select	NP_004351.1:p.Tyr876Phe
NM_001317184.2:c.2444A>T	NP_001304113.1:p.Tyr815Phe
NM_001317185.2:c.1079A>T	NP_001304114.1:p.Tyr360Phe
NM_001317186.2:c.662A>T	NP_001304115.1:p.Tyr221Phe