Canonical Allele Identifier: CA396459035

Gene: CDH1

Linked Data

• dbSNP Id: rs2152131214
• MyVariant Identifiers: chr16:g.68844246T>C (hg19) ; chr16:g.68810343T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68810343T>C , CM000678.2:g.68810343T>C	GRCh38
NC_000016.9:g.68844246T>C , CM000678.1:g.68844246T>C	GRCh37
NC_000016.8:g.67401747T>C	NCBI36
NG_008021.1:g.78052T>C , LRG_301:g.78052T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261769.10:c.832+2T>C MANE Select	ENSP00000261769.4:n.832+2T>C
ENST00000261769.9:c.832+2T>C	ENSP00000261769.4:n.832+2T>C
ENST00000422392.6:c.832+2T>C	ENSP00000414946.2:n.832+2T>C
ENST00000561751.1:c.455-1341T>C
ENST00000562836.5:n.903+2T>C
ENST00000566510.5:c.676+2T>C	ENSP00000458139.1:n.676+2T>C
ENST00000566612.5:c.832+2T>C	ENSP00000454782.1:n.832+2T>C
ENST00000611625.4:c.832+2T>C	ENSP00000481063.1:n.832+2T>C
ENST00000612417.4:c.832+2T>C	ENSP00000478360.1:n.832+2T>C
ENST00000621016.4:c.832+2T>C	ENSP00000480664.1:n.832+2T>C
NM_004360.3:c.832+2T>C , LRG_301t1:c.832+2T>C	NP_004351.1:n.832+2T>C
XM_011523488.1:c.97+2T>C	XP_011521790.1:n.97+2T>C
XM_011523489.1:c.97+2T>C	XP_011521791.1:n.97+2T>C
NM_001317184.1:c.832+2T>C	NP_001304113.1:n.832+2T>C
NM_001317185.1:c.-784+2T>C	NP_001304114.1:n.-784+2T>C
NM_001317186.1:c.-988+2T>C	NP_001304115.1:n.-988+2T>C
NM_004360.4:c.832+2T>C	NP_004351.1:n.832+2T>C
NM_004360.5:c.832+2T>C MANE Select	NP_004351.1:n.832+2T>C
NM_001317184.2:c.832+2T>C	NP_001304113.1:n.832+2T>C
NM_001317185.2:c.-784+2T>C	NP_001304114.1:n.-784+2T>C
NM_001317186.2:c.-988+2T>C	NP_001304115.1:n.-988+2T>C