Canonical Allele Identifier: CA396471224

Gene: CDH1

Linked Data

• ClinVar Variation Id: 1376050
• ClinVar RCV Id: RCV001871177
• dbSNP Id: rs2152142424
• MyVariant Identifiers: chr16:g.68863665G>A (hg19) ; chr16:g.68829762G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68829762G>A , CM000678.2:g.68829762G>A	GRCh38
NC_000016.9:g.68863665G>A , CM000678.1:g.68863665G>A	GRCh37
NC_000016.8:g.67421166G>A	NCBI36
NG_008021.1:g.97471G>A , LRG_301:g.97471G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261769.10:c.2404G>A MANE Select	ENSP00000261769.4:p.Ala802Thr
ENST00000261769.9:c.2404G>A	ENSP00000261769.4:p.Ala802Thr
ENST00000422392.6:c.2221G>A	ENSP00000414946.2:p.Ala741Thr
ENST00000562118.1:n.622G>A
ENST00000562836.5:n.2475G>A
ENST00000566510.5:c.*1070G>A	ENSP00000458139.1:n.*1070G>A
ENST00000566612.5:c.*644G>A	ENSP00000454782.1:n.*644G>A
ENST00000611625.4:c.2467G>A	ENSP00000481063.1:p.Ala823Thr
ENST00000612417.4:c.1853+3208G>A	ENSP00000478360.1:n.1853+3208G>A
ENST00000621016.4:c.1866-4441G>A	ENSP00000480664.1:n.1866-4441G>A
NM_004360.3:c.2404G>A , LRG_301t1:c.2404G>A	NP_004351.1:p.Ala802Thr
XM_011523488.1:c.1669G>A	XP_011521790.1:p.Ala557Thr
XM_011523489.1:c.1669G>A	XP_011521791.1:p.Ala557Thr
NM_001317184.1:c.2221G>A	NP_001304113.1:p.Ala741Thr
NM_001317185.1:c.856G>A	NP_001304114.1:p.Ala286Thr
NM_001317186.1:c.439G>A	NP_001304115.1:p.Ala147Thr
NM_004360.4:c.2404G>A	NP_004351.1:p.Ala802Thr
NM_004360.5:c.2404G>A MANE Select	NP_004351.1:p.Ala802Thr
NM_001317184.2:c.2221G>A	NP_001304113.1:p.Ala741Thr
NM_001317185.2:c.856G>A	NP_001304114.1:p.Ala286Thr
NM_001317186.2:c.439G>A	NP_001304115.1:p.Ala147Thr