Canonical Allele Identifier: CA623574817

Gene: CDH1

Linked Data

• dbSNP Id: rs1416031406
• gnomAD v2: 16-68856173-T-C
• gnomAD v3: 16-68822270-T-C
• gnomAD v4: 16-68822270-T-C
• MyVariant Identifiers: chr16:g.68856173T>C (hg19) ; chr16:g.68822270T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68822270T>C , CM000678.2:g.68822270T>C	GRCh38
NC_000016.9:g.68856173T>C , CM000678.1:g.68856173T>C	GRCh37
NC_000016.8:g.67413674T>C	NCBI36
NG_008021.1:g.89979T>C , LRG_301:g.89979T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261769.10:c.1936+45T>C MANE Select	ENSP00000261769.4:n.1936+45T>C
ENST00000261769.9:c.1936+45T>C	ENSP00000261769.4:n.1936+45T>C
ENST00000422392.6:c.1753+45T>C	ENSP00000414946.2:n.1753+45T>C
ENST00000562836.5:n.2007+45T>C
ENST00000566510.5:c.*602+45T>C	ENSP00000458139.1:n.*602+45T>C
ENST00000566612.5:c.*176+45T>C	ENSP00000454782.1:n.*176+45T>C
ENST00000611625.4:c.1999+45T>C	ENSP00000481063.1:n.1999+45T>C
ENST00000612417.4:c.1830+151T>C	ENSP00000478360.1:n.1830+151T>C
ENST00000621016.4:c.1865+116T>C	ENSP00000480664.1:n.1865+116T>C
NM_004360.3:c.1936+45T>C , LRG_301t1:c.1936+45T>C	NP_004351.1:n.1936+45T>C
XM_011523488.1:c.1201+45T>C	XP_011521790.1:n.1201+45T>C
XM_011523489.1:c.1201+45T>C	XP_011521791.1:n.1201+45T>C
NM_001317184.1:c.1753+45T>C	NP_001304113.1:n.1753+45T>C
NM_001317185.1:c.388+45T>C	NP_001304114.1:n.388+45T>C
NM_001317186.1:c.-30+45T>C	NP_001304115.1:n.-30+45T>C
NM_004360.4:c.1936+45T>C	NP_004351.1:n.1936+45T>C
NM_004360.5:c.1936+45T>C MANE Select	NP_004351.1:n.1936+45T>C
NM_001317184.2:c.1753+45T>C	NP_001304113.1:n.1753+45T>C
NM_001317185.2:c.388+45T>C	NP_001304114.1:n.388+45T>C
NM_001317186.2:c.-30+45T>C	NP_001304115.1:n.-30+45T>C