Canonical Allele Identifier: CA396459808

Gene: CDH1

Linked Data

• dbSNP Id: rs2152132086
• MyVariant Identifiers: chr16:g.68845712A>T (hg19) ; chr16:g.68811809A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68811809A>T , CM000678.2:g.68811809A>T	GRCh38
NC_000016.9:g.68845712A>T , CM000678.1:g.68845712A>T	GRCh37
NC_000016.8:g.67403213A>T	NCBI36
NG_008021.1:g.79518A>T , LRG_301:g.79518A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261769.10:c.958A>T MANE Select	ENSP00000261769.4:p.Asn320Tyr
ENST00000261769.9:c.958A>T	ENSP00000261769.4:p.Asn320Tyr
ENST00000422392.6:c.958A>T	ENSP00000414946.2:p.Asn320Tyr
ENST00000561751.1:c.580A>T
ENST00000562836.5:n.1029A>T
ENST00000566510.5:c.802A>T	ENSP00000458139.1:p.Asn268Tyr
ENST00000566612.5:c.958A>T	ENSP00000454782.1:p.Asn320Tyr
ENST00000611625.4:c.958A>T	ENSP00000481063.1:p.Asn320Tyr
ENST00000612417.4:c.958A>T	ENSP00000478360.1:p.Asn320Tyr
ENST00000621016.4:c.958A>T	ENSP00000480664.1:p.Asn320Tyr
NM_004360.3:c.958A>T , LRG_301t1:c.958A>T	NP_004351.1:p.Asn320Tyr
XM_011523488.1:c.223A>T	XP_011521790.1:p.Asn75Tyr
XM_011523489.1:c.223A>T	XP_011521791.1:p.Asn75Tyr
NM_001317184.1:c.958A>T	NP_001304113.1:p.Asn320Tyr
NM_001317185.1:c.-658A>T	NP_001304114.1:n.-658A>T
NM_001317186.1:c.-862A>T	NP_001304115.1:n.-862A>T
NM_004360.4:c.958A>T	NP_004351.1:p.Asn320Tyr
NM_004360.5:c.958A>T MANE Select	NP_004351.1:p.Asn320Tyr
NM_001317184.2:c.958A>T	NP_001304113.1:p.Asn320Tyr
NM_001317185.2:c.-658A>T	NP_001304114.1:n.-658A>T
NM_001317186.2:c.-862A>T	NP_001304115.1:n.-862A>T