Canonical Allele Identifier: CA396457644

Gene: CDH1

Linked Data

• dbSNP Id: rs1060501213
• MyVariant Identifiers: chr16:g.68842391G>C (hg19) ; chr16:g.68808488G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68808488G>C , CM000678.2:g.68808488G>C	GRCh38
NC_000016.9:g.68842391G>C , CM000678.1:g.68842391G>C	GRCh37
NC_000016.8:g.67399892G>C	NCBI36
NG_008021.1:g.76197G>C , LRG_301:g.76197G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261769.10:c.452G>C MANE Select	ENSP00000261769.4:p.Arg151Thr
ENST00000261769.9:c.452G>C	ENSP00000261769.4:p.Arg151Thr
ENST00000422392.6:c.452G>C	ENSP00000414946.2:p.Arg151Thr
ENST00000561751.1:c.219G>C
ENST00000562836.5:n.523G>C
ENST00000564676.5:n.734G>C
ENST00000564745.1:n.447G>C
ENST00000566510.5:c.452G>C	ENSP00000458139.1:p.Arg151Thr
ENST00000566612.5:c.452G>C	ENSP00000454782.1:p.Arg151Thr
ENST00000611625.4:c.452G>C	ENSP00000481063.1:p.Arg151Thr
ENST00000612417.4:c.452G>C	ENSP00000478360.1:p.Arg151Thr
ENST00000621016.4:c.452G>C	ENSP00000480664.1:p.Arg151Thr
NM_004360.3:c.452G>C , LRG_301t1:c.452G>C	NP_004351.1:p.Arg151Thr
XM_011523488.1:c.-284G>C	XP_011521790.1:n.-284G>C
XM_011523489.1:c.-284G>C	XP_011521791.1:n.-284G>C
NM_001317184.1:c.452G>C	NP_001304113.1:p.Arg151Thr
NM_001317185.1:c.-1164G>C	NP_001304114.1:n.-1164G>C
NM_001317186.1:c.-1368G>C	NP_001304115.1:n.-1368G>C
NM_004360.4:c.452G>C	NP_004351.1:p.Arg151Thr
NM_004360.5:c.452G>C MANE Select	NP_004351.1:p.Arg151Thr
NM_001317184.2:c.452G>C	NP_001304113.1:p.Arg151Thr
NM_001317185.2:c.-1164G>C	NP_001304114.1:n.-1164G>C
NM_001317186.2:c.-1368G>C	NP_001304115.1:n.-1368G>C