Canonical Allele Identifier: CA396472378

Gene: CDH1

Linked Data

• ClinVar Variation Id: 1023240
• ClinVar RCV Id: RCV001323255
• dbSNP Id: rs1961539722
• MyVariant Identifiers: chr16:g.68867299A>G (hg19) ; chr16:g.68833396A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68833396A>G , CM000678.2:g.68833396A>G	GRCh38
NC_000016.9:g.68867299A>G , CM000678.1:g.68867299A>G	GRCh37
NC_000016.8:g.67424800A>G	NCBI36
NG_008021.1:g.101105A>G , LRG_301:g.101105A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261769.10:c.2546A>G MANE Select	ENSP00000261769.4:p.Asn849Ser
ENST00000261769.9:c.2546A>G	ENSP00000261769.4:p.Asn849Ser
ENST00000422392.6:c.2363A>G	ENSP00000414946.2:p.Asn788Ser
ENST00000562118.1:n.764A>G
ENST00000562836.5:n.2617A>G
ENST00000566510.5:c.*1212A>G	ENSP00000458139.1:n.*1212A>G
ENST00000566612.5:c.*786A>G	ENSP00000454782.1:n.*786A>G
ENST00000611625.4:c.2609A>G	ENSP00000481063.1:p.Asn870Ser
ENST00000612417.4:c.1854-795A>G	ENSP00000478360.1:n.1854-795A>G
ENST00000621016.4:c.1866-807A>G	ENSP00000480664.1:n.1866-807A>G
NM_004360.3:c.2546A>G , LRG_301t1:c.2546A>G	NP_004351.1:p.Asn849Ser
XM_011523488.1:c.1811A>G	XP_011521790.1:p.Asn604Ser
XM_011523489.1:c.1811A>G	XP_011521791.1:p.Asn604Ser
NM_001317184.1:c.2363A>G	NP_001304113.1:p.Asn788Ser
NM_001317185.1:c.998A>G	NP_001304114.1:p.Asn333Ser
NM_001317186.1:c.581A>G	NP_001304115.1:p.Asn194Ser
NM_004360.4:c.2546A>G	NP_004351.1:p.Asn849Ser
NM_004360.5:c.2546A>G MANE Select	NP_004351.1:p.Asn849Ser
NM_001317184.2:c.2363A>G	NP_001304113.1:p.Asn788Ser
NM_001317185.2:c.998A>G	NP_001304114.1:p.Asn333Ser
NM_001317186.2:c.581A>G	NP_001304115.1:p.Asn194Ser