Canonical Allele Identifier: CA396462900

Gene: CDH1

Linked Data

• MyVariant Identifiers: chr16:g.68849494T>A (hg19) ; chr16:g.68815591T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68815591T>A , CM000678.2:g.68815591T>A	GRCh38
NC_000016.9:g.68849494T>A , CM000678.1:g.68849494T>A	GRCh37
NC_000016.8:g.67406995T>A	NCBI36
NG_008021.1:g.83300T>A , LRG_301:g.83300T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000261769.10:c.1397T>A MANE Select	ENSP00000261769.4:p.Leu466His
ENST00000261769.9:c.1397T>A	ENSP00000261769.4:p.Leu466His
ENST00000422392.6:c.1214T>A	ENSP00000414946.2:p.Leu405His
ENST00000562836.5:n.1468T>A
ENST00000566510.5:c.*63T>A	ENSP00000458139.1:n.*63T>A
ENST00000566612.5:c.1397T>A	ENSP00000454782.1:p.Leu466His
ENST00000611625.4:c.1460T>A	ENSP00000481063.1:p.Leu487His
ENST00000612417.4:c.1397T>A	ENSP00000478360.1:p.Leu466His
ENST00000621016.4:c.1397T>A	ENSP00000480664.1:p.Leu466His
NM_004360.3:c.1397T>A , LRG_301t1:c.1397T>A	NP_004351.1:p.Leu466His
XM_011523488.1:c.662T>A	XP_011521790.1:p.Leu221His
XM_011523489.1:c.662T>A	XP_011521791.1:p.Leu221His
NM_001317184.1:c.1214T>A	NP_001304113.1:p.Leu405His
NM_001317185.1:c.-152T>A	NP_001304114.1:n.-152T>A
NM_001317186.1:c.-423T>A	NP_001304115.1:n.-423T>A
NM_004360.4:c.1397T>A	NP_004351.1:p.Leu466His
NM_004360.5:c.1397T>A MANE Select	NP_004351.1:p.Leu466His
NM_001317184.2:c.1214T>A	NP_001304113.1:p.Leu405His
NM_001317185.2:c.-152T>A	NP_001304114.1:n.-152T>A
NM_001317186.2:c.-423T>A	NP_001304115.1:n.-423T>A