Canonical Allele Identifier: CA496154375

Gene: CDH1

Linked Data

• MyVariant Identifiers: chr16:g.68853249T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68819346T>G , CM000678.2:g.68819346T>G	GRCh38
NC_000016.9:g.68853249T>G , CM000678.1:g.68853249T>G	GRCh37
NC_000016.8:g.67410750T>G	NCBI36
NG_008021.1:g.87055T>G , LRG_301:g.87055T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261769.10:c.1632T>G MANE Select	ENSP00000261769.4:p.Thr544=
ENST00000261769.9:c.1632T>G	ENSP00000261769.4:p.Thr544=
ENST00000422392.6:c.1449T>G	ENSP00000414946.2:p.Thr483=
ENST00000562836.5:n.1703T>G
ENST00000566510.5:c.*298T>G	ENSP00000458139.1:n.*298T>G
ENST00000566612.5:c.1566-2655T>G	ENSP00000454782.1:n.1566-2655T>G
ENST00000611625.4:c.1695T>G	ENSP00000481063.1:p.Thr565=
ENST00000612417.4:c.1632T>G	ENSP00000478360.1:p.Thr544=
ENST00000621016.4:c.1632T>G	ENSP00000480664.1:p.Thr544=
NM_004360.3:c.1632T>G , LRG_301t1:c.1632T>G	NP_004351.1:p.Thr544=
XM_011523488.1:c.897T>G	XP_011521790.1:p.Thr299=
XM_011523489.1:c.897T>G	XP_011521791.1:p.Thr299=
NM_001317184.1:c.1449T>G	NP_001304113.1:p.Thr483=
NM_001317185.1:c.84T>G	NP_001304114.1:p.Thr28=
NM_001317186.1:c.-254-2655T>G	NP_001304115.1:n.-254-2655T>G
NM_004360.4:c.1632T>G	NP_004351.1:p.Thr544=
NM_004360.5:c.1632T>G MANE Select	NP_004351.1:p.Thr544=
NM_001317184.2:c.1449T>G	NP_001304113.1:p.Thr483=
NM_001317185.2:c.84T>G	NP_001304114.1:p.Thr28=
NM_001317186.2:c.-254-2655T>G	NP_001304115.1:n.-254-2655T>G