Canonical Allele Identifier: CA496392587

Gene: CDH1

Linked Data

• dbSNP Id: rs2152138359
• MyVariant Identifiers: chr16:g.68856007G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68822104G>A , CM000678.2:g.68822104G>A	GRCh38
NC_000016.9:g.68856007G>A , CM000678.1:g.68856007G>A	GRCh37
NC_000016.8:g.67413508G>A	NCBI36
NG_008021.1:g.89813G>A , LRG_301:g.89813G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261769.10:c.1815G>A MANE Select	ENSP00000261769.4:p.Arg605=
ENST00000261769.9:c.1815G>A	ENSP00000261769.4:p.Arg605=
ENST00000422392.6:c.1632G>A	ENSP00000414946.2:p.Arg544=
ENST00000562836.5:n.1886G>A
ENST00000566510.5:c.*481G>A	ENSP00000458139.1:n.*481G>A
ENST00000566612.5:c.*55G>A	ENSP00000454782.1:n.*55G>A
ENST00000611625.4:c.1878G>A	ENSP00000481063.1:p.Arg626=
ENST00000612417.4:c.1815G>A	ENSP00000478360.1:p.Arg605=
ENST00000621016.4:c.1815G>A	ENSP00000480664.1:p.Arg605=
NM_004360.3:c.1815G>A , LRG_301t1:c.1815G>A	NP_004351.1:p.Arg605=
XM_011523488.1:c.1080G>A	XP_011521790.1:p.Arg360=
XM_011523489.1:c.1080G>A	XP_011521791.1:p.Arg360=
NM_001317184.1:c.1632G>A	NP_001304113.1:p.Arg544=
NM_001317185.1:c.267G>A	NP_001304114.1:p.Arg89=
NM_001317186.1:c.-151G>A	NP_001304115.1:n.-151G>A
NM_004360.4:c.1815G>A	NP_004351.1:p.Arg605=
NM_004360.5:c.1815G>A MANE Select	NP_004351.1:p.Arg605=
NM_001317184.2:c.1632G>A	NP_001304113.1:p.Arg544=
NM_001317185.2:c.267G>A	NP_001304114.1:p.Arg89=
NM_001317186.2:c.-151G>A	NP_001304115.1:n.-151G>A