Canonical Allele Identifier: CA496157380

Gene: CDH1

Linked Data

• MyVariant Identifiers: chr16:g.68863589G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68829686G>T , CM000678.2:g.68829686G>T	GRCh38
NC_000016.9:g.68863589G>T , CM000678.1:g.68863589G>T	GRCh37
NC_000016.8:g.67421090G>T	NCBI36
NG_008021.1:g.97395G>T , LRG_301:g.97395G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000261769.10:c.2328G>T MANE Select	ENSP00000261769.4:p.Leu776=
ENST00000261769.9:c.2328G>T	ENSP00000261769.4:p.Leu776=
ENST00000422392.6:c.2145G>T	ENSP00000414946.2:p.Leu715=
ENST00000562118.1:n.546G>T
ENST00000562836.5:n.2399G>T
ENST00000566510.5:c.*994G>T	ENSP00000458139.1:n.*994G>T
ENST00000566612.5:c.*568G>T	ENSP00000454782.1:n.*568G>T
ENST00000611625.4:c.2391G>T	ENSP00000481063.1:p.Leu797=
ENST00000612417.4:c.1853+3132G>T	ENSP00000478360.1:n.1853+3132G>T
ENST00000621016.4:c.1866-4517G>T	ENSP00000480664.1:n.1866-4517G>T
NM_004360.3:c.2328G>T , LRG_301t1:c.2328G>T	NP_004351.1:p.Leu776=
XM_011523488.1:c.1593G>T	XP_011521790.1:p.Leu531=
XM_011523489.1:c.1593G>T	XP_011521791.1:p.Leu531=
NM_001317184.1:c.2145G>T	NP_001304113.1:p.Leu715=
NM_001317185.1:c.780G>T	NP_001304114.1:p.Leu260=
NM_001317186.1:c.363G>T	NP_001304115.1:p.Leu121=
NM_004360.4:c.2328G>T	NP_004351.1:p.Leu776=
NM_004360.5:c.2328G>T MANE Select	NP_004351.1:p.Leu776=
NM_001317184.2:c.2145G>T	NP_001304113.1:p.Leu715=
NM_001317185.2:c.780G>T	NP_001304114.1:p.Leu260=
NM_001317186.2:c.363G>T	NP_001304115.1:p.Leu121=