Canonical Allele Identifier: CA396462832

Gene: CDH1

Linked Data

• MyVariant Identifiers: chr16:g.68849473T>G (hg19) ; chr16:g.68815570T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68815570T>G , CM000678.2:g.68815570T>G	GRCh38
NC_000016.9:g.68849473T>G , CM000678.1:g.68849473T>G	GRCh37
NC_000016.8:g.67406974T>G	NCBI36
NG_008021.1:g.83279T>G , LRG_301:g.83279T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261769.10:c.1376T>G MANE Select	ENSP00000261769.4:p.Val459Gly
ENST00000261769.9:c.1376T>G	ENSP00000261769.4:p.Val459Gly
ENST00000422392.6:c.1193T>G	ENSP00000414946.2:p.Val398Gly
ENST00000562836.5:n.1447T>G
ENST00000566510.5:c.*42T>G	ENSP00000458139.1:n.*42T>G
ENST00000566612.5:c.1376T>G	ENSP00000454782.1:p.Val459Gly
ENST00000611625.4:c.1439T>G	ENSP00000481063.1:p.Val480Gly
ENST00000612417.4:c.1376T>G	ENSP00000478360.1:p.Val459Gly
ENST00000621016.4:c.1376T>G	ENSP00000480664.1:p.Val459Gly
NM_004360.3:c.1376T>G , LRG_301t1:c.1376T>G	NP_004351.1:p.Val459Gly
XM_011523488.1:c.641T>G	XP_011521790.1:p.Val214Gly
XM_011523489.1:c.641T>G	XP_011521791.1:p.Val214Gly
NM_001317184.1:c.1193T>G	NP_001304113.1:p.Val398Gly
NM_001317185.1:c.-173T>G	NP_001304114.1:n.-173T>G
NM_001317186.1:c.-444T>G	NP_001304115.1:n.-444T>G
NM_004360.4:c.1376T>G	NP_004351.1:p.Val459Gly
NM_004360.5:c.1376T>G MANE Select	NP_004351.1:p.Val459Gly
NM_001317184.2:c.1193T>G	NP_001304113.1:p.Val398Gly
NM_001317185.2:c.-173T>G	NP_001304114.1:n.-173T>G
NM_001317186.2:c.-444T>G	NP_001304115.1:n.-444T>G