Canonical Allele Identifier: CA396467567

Gene: CDH1

Linked Data

• dbSNP Id: rs2152139283
• MyVariant Identifiers: chr16:g.68857333G>A (hg19) ; chr16:g.68823430G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68823430G>A , CM000678.2:g.68823430G>A	GRCh38
NC_000016.9:g.68857333G>A , CM000678.1:g.68857333G>A	GRCh37
NC_000016.8:g.67414834G>A	NCBI36
NG_008021.1:g.91139G>A , LRG_301:g.91139G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261769.10:c.1968G>A MANE Select	ENSP00000261769.4:p.Met656Ile
ENST00000261769.9:c.1968G>A	ENSP00000261769.4:p.Met656Ile
ENST00000422392.6:c.1785G>A	ENSP00000414946.2:p.Met595Ile
ENST00000562118.1:n.186G>A
ENST00000562836.5:n.2039G>A
ENST00000566510.5:c.*634G>A	ENSP00000458139.1:n.*634G>A
ENST00000566612.5:c.*208G>A	ENSP00000454782.1:n.*208G>A
ENST00000611625.4:c.2031G>A	ENSP00000481063.1:p.Met677Ile
ENST00000612417.4:c.1830+1311G>A	ENSP00000478360.1:n.1830+1311G>A
ENST00000621016.4:c.1865+1276G>A	ENSP00000480664.1:n.1865+1276G>A
NM_004360.3:c.1968G>A , LRG_301t1:c.1968G>A	NP_004351.1:p.Met656Ile
XM_011523488.1:c.1233G>A	XP_011521790.1:p.Met411Ile
XM_011523489.1:c.1233G>A	XP_011521791.1:p.Met411Ile
NM_001317184.1:c.1785G>A	NP_001304113.1:p.Met595Ile
NM_001317185.1:c.420G>A	NP_001304114.1:p.Met140Ile
NM_001317186.1:c.3G>A	NP_001304115.1:p.Met1Ile
NM_004360.4:c.1968G>A	NP_004351.1:p.Met656Ile
NM_004360.5:c.1968G>A MANE Select	NP_004351.1:p.Met656Ile
NM_001317184.2:c.1785G>A	NP_001304113.1:p.Met595Ile
NM_001317185.2:c.420G>A	NP_001304114.1:p.Met140Ile
NM_001317186.2:c.3G>A	NP_001304115.1:p.Met1Ile