Canonical Allele Identifier: CA396467085

Gene: CDH1

Linked Data

• MyVariant Identifiers: chr16:g.68856063C>A (hg19) ; chr16:g.68822160C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68822160C>A , CM000678.2:g.68822160C>A	GRCh38
NC_000016.9:g.68856063C>A , CM000678.1:g.68856063C>A	GRCh37
NC_000016.8:g.67413564C>A	NCBI36
NG_008021.1:g.89869C>A , LRG_301:g.89869C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000261769.10:c.1871C>A MANE Select	ENSP00000261769.4:p.Ser624Tyr
ENST00000261769.9:c.1871C>A	ENSP00000261769.4:p.Ser624Tyr
ENST00000422392.6:c.1688C>A	ENSP00000414946.2:p.Ser563Tyr
ENST00000562836.5:n.1942C>A
ENST00000566510.5:c.*537C>A	ENSP00000458139.1:n.*537C>A
ENST00000566612.5:c.*111C>A	ENSP00000454782.1:n.*111C>A
ENST00000611625.4:c.1934C>A	ENSP00000481063.1:p.Ser645Tyr
ENST00000612417.4:c.1830+41C>A	ENSP00000478360.1:n.1830+41C>A
ENST00000621016.4:c.1865+6C>A	ENSP00000480664.1:n.1865+6C>A
NM_004360.3:c.1871C>A , LRG_301t1:c.1871C>A	NP_004351.1:p.Ser624Tyr
XM_011523488.1:c.1136C>A	XP_011521790.1:p.Ser379Tyr
XM_011523489.1:c.1136C>A	XP_011521791.1:p.Ser379Tyr
NM_001317184.1:c.1688C>A	NP_001304113.1:p.Ser563Tyr
NM_001317185.1:c.323C>A	NP_001304114.1:p.Ser108Tyr
NM_001317186.1:c.-95C>A	NP_001304115.1:n.-95C>A
NM_004360.4:c.1871C>A	NP_004351.1:p.Ser624Tyr
NM_004360.5:c.1871C>A MANE Select	NP_004351.1:p.Ser624Tyr
NM_001317184.2:c.1688C>A	NP_001304113.1:p.Ser563Tyr
NM_001317185.2:c.323C>A	NP_001304114.1:p.Ser108Tyr
NM_001317186.2:c.-95C>A	NP_001304115.1:n.-95C>A