Canonical Allele Identifier: CA396467114

Gene: CDH1

Linked Data

• dbSNP Id: rs1555516886
• MyVariant Identifiers: chr16:g.68856071A>T (hg19) ; chr16:g.68822168A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68822168A>T , CM000678.2:g.68822168A>T	GRCh38
NC_000016.9:g.68856071A>T , CM000678.1:g.68856071A>T	GRCh37
NC_000016.8:g.67413572A>T	NCBI36
NG_008021.1:g.89877A>T , LRG_301:g.89877A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261769.10:c.1879A>T MANE Select	ENSP00000261769.4:p.Thr627Ser
ENST00000261769.9:c.1879A>T	ENSP00000261769.4:p.Thr627Ser
ENST00000422392.6:c.1696A>T	ENSP00000414946.2:p.Thr566Ser
ENST00000562836.5:n.1950A>T
ENST00000566510.5:c.*545A>T	ENSP00000458139.1:n.*545A>T
ENST00000566612.5:c.*119A>T	ENSP00000454782.1:n.*119A>T
ENST00000611625.4:c.1942A>T	ENSP00000481063.1:p.Thr648Ser
ENST00000612417.4:c.1830+49A>T	ENSP00000478360.1:n.1830+49A>T
ENST00000621016.4:c.1865+14A>T	ENSP00000480664.1:n.1865+14A>T
NM_004360.3:c.1879A>T , LRG_301t1:c.1879A>T	NP_004351.1:p.Thr627Ser
XM_011523488.1:c.1144A>T	XP_011521790.1:p.Thr382Ser
XM_011523489.1:c.1144A>T	XP_011521791.1:p.Thr382Ser
NM_001317184.1:c.1696A>T	NP_001304113.1:p.Thr566Ser
NM_001317185.1:c.331A>T	NP_001304114.1:p.Thr111Ser
NM_001317186.1:c.-87A>T	NP_001304115.1:n.-87A>T
NM_004360.4:c.1879A>T	NP_004351.1:p.Thr627Ser
NM_004360.5:c.1879A>T MANE Select	NP_004351.1:p.Thr627Ser
NM_001317184.2:c.1696A>T	NP_001304113.1:p.Thr566Ser
NM_001317185.2:c.331A>T	NP_001304114.1:p.Thr111Ser
NM_001317186.2:c.-87A>T	NP_001304115.1:n.-87A>T