Canonical Allele Identifier: CA396472813

Gene: CDH1

Linked Data

• ClinVar Variation Id: 1035849
• ClinVar RCV Id: RCV001338776
• dbSNP Id: rs900118000
• gnomAD v4: 16-68833474-T-C
• MyVariant Identifiers: chr16:g.68867377T>C (hg19) ; chr16:g.68833474T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68833474T>C , CM000678.2:g.68833474T>C	GRCh38
NC_000016.9:g.68867377T>C , CM000678.1:g.68867377T>C	GRCh37
NC_000016.8:g.67424878T>C	NCBI36
NG_008021.1:g.101183T>C , LRG_301:g.101183T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261769.10:c.2624T>C MANE Select	ENSP00000261769.4:p.Met875Thr
ENST00000261769.9:c.2624T>C	ENSP00000261769.4:p.Met875Thr
ENST00000422392.6:c.2441T>C	ENSP00000414946.2:p.Met814Thr
ENST00000562118.1:n.842T>C
ENST00000562836.5:n.2695T>C
ENST00000566510.5:c.*1290T>C	ENSP00000458139.1:n.*1290T>C
ENST00000566612.5:c.*864T>C	ENSP00000454782.1:n.*864T>C
ENST00000611625.4:c.2687T>C	ENSP00000481063.1:p.Met896Thr
ENST00000612417.4:c.1854-717T>C	ENSP00000478360.1:n.1854-717T>C
ENST00000621016.4:c.1866-729T>C	ENSP00000480664.1:n.1866-729T>C
NM_004360.3:c.2624T>C , LRG_301t1:c.2624T>C	NP_004351.1:p.Met875Thr
XM_011523488.1:c.1889T>C	XP_011521790.1:p.Met630Thr
XM_011523489.1:c.1889T>C	XP_011521791.1:p.Met630Thr
NM_001317184.1:c.2441T>C	NP_001304113.1:p.Met814Thr
NM_001317185.1:c.1076T>C	NP_001304114.1:p.Met359Thr
NM_001317186.1:c.659T>C	NP_001304115.1:p.Met220Thr
NM_004360.4:c.2624T>C	NP_004351.1:p.Met875Thr
NM_004360.5:c.2624T>C MANE Select	NP_004351.1:p.Met875Thr
NM_001317184.2:c.2441T>C	NP_001304113.1:p.Met814Thr
NM_001317185.2:c.1076T>C	NP_001304114.1:p.Met359Thr
NM_001317186.2:c.659T>C	NP_001304115.1:p.Met220Thr