Canonical Allele Identifier: CA496152761

Gene: CDH1

Linked Data

• ClinVar Variation Id: 491555
• ClinVar RCV Id: RCV000584529
• dbSNP Id: rs1555515428
• MyVariant Identifiers: chr16:g.68844114T>G (hg19) ; chr16:g.68810211T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68810211T>G , CM000678.2:g.68810211T>G	GRCh38
NC_000016.9:g.68844114T>G , CM000678.1:g.68844114T>G	GRCh37
NC_000016.8:g.67401615T>G	NCBI36
NG_008021.1:g.77920T>G , LRG_301:g.77920T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000261769.10:c.702T>G MANE Select	ENSP00000261769.4:p.Ala234=
ENST00000261769.9:c.702T>G	ENSP00000261769.4:p.Ala234=
ENST00000422392.6:c.702T>G	ENSP00000414946.2:p.Ala234=
ENST00000561751.1:c.454+1363T>G
ENST00000562836.5:n.773T>G
ENST00000566510.5:c.546T>G	ENSP00000458139.1:p.Ala182=
ENST00000566612.5:c.702T>G	ENSP00000454782.1:p.Ala234=
ENST00000611625.4:c.702T>G	ENSP00000481063.1:p.Ala234=
ENST00000612417.4:c.702T>G	ENSP00000478360.1:p.Ala234=
ENST00000621016.4:c.702T>G	ENSP00000480664.1:p.Ala234=
NM_004360.3:c.702T>G , LRG_301t1:c.702T>G	NP_004351.1:p.Ala234=
XM_011523488.1:c.-34T>G	XP_011521790.1:n.-34T>G
XM_011523489.1:c.-34T>G	XP_011521791.1:n.-34T>G
NM_001317184.1:c.702T>G	NP_001304113.1:p.Ala234=
NM_001317185.1:c.-914T>G	NP_001304114.1:n.-914T>G
NM_001317186.1:c.-1118T>G	NP_001304115.1:n.-1118T>G
NM_004360.4:c.702T>G	NP_004351.1:p.Ala234=
NM_004360.5:c.702T>G MANE Select	NP_004351.1:p.Ala234=
NM_001317184.2:c.702T>G	NP_001304113.1:p.Ala234=
NM_001317185.2:c.-914T>G	NP_001304114.1:n.-914T>G
NM_001317186.2:c.-1118T>G	NP_001304115.1:n.-1118T>G