Canonical Allele Identifier: CA496393191

Gene: CDH1

Linked Data

• dbSNP Id: rs2152144128
• gnomAD v4: 16-68833433-C-T
• MyVariant Identifiers: chr16:g.68867336C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68833433C>T , CM000678.2:g.68833433C>T	GRCh38
NC_000016.9:g.68867336C>T , CM000678.1:g.68867336C>T	GRCh37
NC_000016.8:g.67424837C>T	NCBI36
NG_008021.1:g.101142C>T , LRG_301:g.101142C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261769.10:c.2583C>T MANE Select	ENSP00000261769.4:p.Tyr861=
ENST00000261769.9:c.2583C>T	ENSP00000261769.4:p.Tyr861=
ENST00000422392.6:c.2400C>T	ENSP00000414946.2:p.Tyr800=
ENST00000562118.1:n.801C>T
ENST00000562836.5:n.2654C>T
ENST00000566510.5:c.*1249C>T	ENSP00000458139.1:n.*1249C>T
ENST00000566612.5:c.*823C>T	ENSP00000454782.1:n.*823C>T
ENST00000611625.4:c.2646C>T	ENSP00000481063.1:p.Tyr882=
ENST00000612417.4:c.1854-758C>T	ENSP00000478360.1:n.1854-758C>T
ENST00000621016.4:c.1866-770C>T	ENSP00000480664.1:n.1866-770C>T
NM_004360.3:c.2583C>T , LRG_301t1:c.2583C>T	NP_004351.1:p.Tyr861=
XM_011523488.1:c.1848C>T	XP_011521790.1:p.Tyr616=
XM_011523489.1:c.1848C>T	XP_011521791.1:p.Tyr616=
NM_001317184.1:c.2400C>T	NP_001304113.1:p.Tyr800=
NM_001317185.1:c.1035C>T	NP_001304114.1:p.Tyr345=
NM_001317186.1:c.618C>T	NP_001304115.1:p.Tyr206=
NM_004360.4:c.2583C>T	NP_004351.1:p.Tyr861=
NM_004360.5:c.2583C>T MANE Select	NP_004351.1:p.Tyr861=
NM_001317184.2:c.2400C>T	NP_001304113.1:p.Tyr800=
NM_001317185.2:c.1035C>T	NP_001304114.1:p.Tyr345=
NM_001317186.2:c.618C>T	NP_001304115.1:p.Tyr206=