Canonical Allele Identifier: CA396472049

Gene: CDH1

Linked Data

• dbSNP Id: rs2152143890
• MyVariant Identifiers: chr16:g.68867226C>G (hg19) ; chr16:g.68833323C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68833323C>G , CM000678.2:g.68833323C>G	GRCh38
NC_000016.9:g.68867226C>G , CM000678.1:g.68867226C>G	GRCh37
NC_000016.8:g.67424727C>G	NCBI36
NG_008021.1:g.101032C>G , LRG_301:g.101032C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261769.10:c.2473C>G MANE Select	ENSP00000261769.4:p.Pro825Ala
ENST00000261769.9:c.2473C>G	ENSP00000261769.4:p.Pro825Ala
ENST00000422392.6:c.2290C>G	ENSP00000414946.2:p.Pro764Ala
ENST00000562118.1:n.691C>G
ENST00000562836.5:n.2544C>G
ENST00000566510.5:c.*1139C>G	ENSP00000458139.1:n.*1139C>G
ENST00000566612.5:c.*713C>G	ENSP00000454782.1:n.*713C>G
ENST00000611625.4:c.2536C>G	ENSP00000481063.1:p.Pro846Ala
ENST00000612417.4:c.1854-868C>G	ENSP00000478360.1:n.1854-868C>G
ENST00000621016.4:c.1866-880C>G	ENSP00000480664.1:n.1866-880C>G
NM_004360.3:c.2473C>G , LRG_301t1:c.2473C>G	NP_004351.1:p.Pro825Ala
XM_011523488.1:c.1738C>G	XP_011521790.1:p.Pro580Ala
XM_011523489.1:c.1738C>G	XP_011521791.1:p.Pro580Ala
NM_001317184.1:c.2290C>G	NP_001304113.1:p.Pro764Ala
NM_001317185.1:c.925C>G	NP_001304114.1:p.Pro309Ala
NM_001317186.1:c.508C>G	NP_001304115.1:p.Pro170Ala
NM_004360.4:c.2473C>G	NP_004351.1:p.Pro825Ala
NM_004360.5:c.2473C>G MANE Select	NP_004351.1:p.Pro825Ala
NM_001317184.2:c.2290C>G	NP_001304113.1:p.Pro764Ala
NM_001317185.2:c.925C>G	NP_001304114.1:p.Pro309Ala
NM_001317186.2:c.508C>G	NP_001304115.1:p.Pro170Ala