Canonical Allele Identifier: CA396467557

Gene: CDH1

Linked Data

• MyVariant Identifiers: chr16:g.68857329A>G (hg19) ; chr16:g.68823426A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68823426A>G , CM000678.2:g.68823426A>G	GRCh38
NC_000016.9:g.68857329A>G , CM000678.1:g.68857329A>G	GRCh37
NC_000016.8:g.67414830A>G	NCBI36
NG_008021.1:g.91135A>G , LRG_301:g.91135A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261769.10:c.1964A>G MANE Select	ENSP00000261769.4:p.Lys655Arg
ENST00000261769.9:c.1964A>G	ENSP00000261769.4:p.Lys655Arg
ENST00000422392.6:c.1781A>G	ENSP00000414946.2:p.Lys594Arg
ENST00000562118.1:n.182A>G
ENST00000562836.5:n.2035A>G
ENST00000566510.5:c.*630A>G	ENSP00000458139.1:n.*630A>G
ENST00000566612.5:c.*204A>G	ENSP00000454782.1:n.*204A>G
ENST00000611625.4:c.2027A>G	ENSP00000481063.1:p.Lys676Arg
ENST00000612417.4:c.1830+1307A>G	ENSP00000478360.1:n.1830+1307A>G
ENST00000621016.4:c.1865+1272A>G	ENSP00000480664.1:n.1865+1272A>G
NM_004360.3:c.1964A>G , LRG_301t1:c.1964A>G	NP_004351.1:p.Lys655Arg
XM_011523488.1:c.1229A>G	XP_011521790.1:p.Lys410Arg
XM_011523489.1:c.1229A>G	XP_011521791.1:p.Lys410Arg
NM_001317184.1:c.1781A>G	NP_001304113.1:p.Lys594Arg
NM_001317185.1:c.416A>G	NP_001304114.1:p.Lys139Arg
NM_001317186.1:c.-2A>G	NP_001304115.1:n.-2A>G
NM_004360.4:c.1964A>G	NP_004351.1:p.Lys655Arg
NM_004360.5:c.1964A>G MANE Select	NP_004351.1:p.Lys655Arg
NM_001317184.2:c.1781A>G	NP_001304113.1:p.Lys594Arg
NM_001317185.2:c.416A>G	NP_001304114.1:p.Lys139Arg
NM_001317186.2:c.-2A>G	NP_001304115.1:n.-2A>G