Canonical Allele Identifier: CA396467589

Gene: CDH1

Linked Data

• dbSNP Id: rs769844369
• MyVariant Identifiers: chr16:g.68857343G>T (hg19) ; chr16:g.68823440G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68823440G>T , CM000678.2:g.68823440G>T	GRCh38
NC_000016.9:g.68857343G>T , CM000678.1:g.68857343G>T	GRCh37
NC_000016.8:g.67414844G>T	NCBI36
NG_008021.1:g.91149G>T , LRG_301:g.91149G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261769.10:c.1978G>T MANE Select	ENSP00000261769.4:p.Val660Leu
ENST00000261769.9:c.1978G>T	ENSP00000261769.4:p.Val660Leu
ENST00000422392.6:c.1795G>T	ENSP00000414946.2:p.Val599Leu
ENST00000562118.1:n.196G>T
ENST00000562836.5:n.2049G>T
ENST00000566510.5:c.*644G>T	ENSP00000458139.1:n.*644G>T
ENST00000566612.5:c.*218G>T	ENSP00000454782.1:n.*218G>T
ENST00000611625.4:c.2041G>T	ENSP00000481063.1:p.Val681Leu
ENST00000612417.4:c.1830+1321G>T	ENSP00000478360.1:n.1830+1321G>T
ENST00000621016.4:c.1865+1286G>T	ENSP00000480664.1:n.1865+1286G>T
NM_004360.3:c.1978G>T , LRG_301t1:c.1978G>T	NP_004351.1:p.Val660Leu
XM_011523488.1:c.1243G>T	XP_011521790.1:p.Val415Leu
XM_011523489.1:c.1243G>T	XP_011521791.1:p.Val415Leu
NM_001317184.1:c.1795G>T	NP_001304113.1:p.Val599Leu
NM_001317185.1:c.430G>T	NP_001304114.1:p.Val144Leu
NM_001317186.1:c.13G>T	NP_001304115.1:p.Val5Leu
NM_004360.4:c.1978G>T	NP_004351.1:p.Val660Leu
NM_004360.5:c.1978G>T MANE Select	NP_004351.1:p.Val660Leu
NM_001317184.2:c.1795G>T	NP_001304113.1:p.Val599Leu
NM_001317185.2:c.430G>T	NP_001304114.1:p.Val144Leu
NM_001317186.2:c.13G>T	NP_001304115.1:p.Val5Leu