Canonical Allele Identifier: CA375777016

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140671282C>G (hg19) ; chr9:g.137776830C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137776830C>G , CM000671.2:g.137776830C>G	GRCh38
NC_000009.11:g.140671282C>G , CM000671.1:g.140671282C>G	GRCh37
NC_000009.10:g.139791103C>G	NCBI36
NG_011776.1:g.162839C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.2004C>G MANE Select	ENSP00000417980.1:p.Asp668Glu
ENST00000636027.1:c.1890C>G	ENSP00000489961.1:p.Asp630Glu
ENST00000637161.1:c.1911C>G	ENSP00000490328.1:p.Asp637Glu
ENST00000637261.1:c.2044C>G	ENSP00000490815.1:n.2044C>G
ENST00000638071.1:c.1631C>G
ENST00000640639.1:c.1173C>G	ENSP00000491823.1:p.Asp391Glu
ENST00000371394.6:c.*1739C>G	ENSP00000485945.1:n.*1739C>G
ENST00000460843.5:c.2004C>G	ENSP00000417980.1:p.Asp668Glu
ENST00000462484.5:c.2004C>G	ENSP00000417328.1:p.Asp668Glu
ENST00000462942.3:c.861C>G	ENSP00000436107.1:p.Asp287Glu
ENST00000626603.1:n.1619G>C
NM_001145527.1:c.2004C>G	NP_001138999.1:p.Asp668Glu
NM_024757.4:c.2004C>G	NP_079033.4:p.Asp668Glu
XM_005266105.3:c.1995C>G	XP_005266162.1:p.Asp665Glu
XM_005266110.1:c.1911C>G	XP_005266167.1:p.Asp637Glu
XM_006717288.2:c.1986C>G	XP_006717351.1:p.Asp662Glu
XM_011519021.1:c.2013C>G	XP_011517323.1:p.Asp671Glu
XM_011519022.1:c.2010C>G	XP_011517324.1:p.Asp670Glu
XM_011519023.1:c.1992C>G	XP_011517325.1:p.Asp664Glu
XM_011519024.1:c.1935C>G	XP_011517326.1:p.Asp645Glu
XM_011519025.1:c.1911C>G	XP_011517327.1:p.Asp637Glu
XM_011519026.1:c.1869C>G	XP_011517328.1:p.Asp623Glu
XM_011519027.1:c.2013C>G	XP_011517329.1:p.Asp671Glu
XM_011519028.1:c.2013C>G	XP_011517330.1:p.Asp671Glu
XM_011519029.1:c.435C>G	XP_011517331.1:p.Asp145Glu
XM_011519033.1:c.1848C>G	XP_011517335.1:p.Asp616Glu
NM_001354259.1:c.1911C>G	NP_001341188.1:p.Asp637Glu
NM_001354263.1:c.1983C>G	NP_001341192.1:p.Asp661Glu
XM_005266105.5:c.1995C>G	XP_005266162.1:p.Asp665Glu
XM_011519021.3:c.2013C>G	XP_011517323.1:p.Asp671Glu
XM_011519022.3:c.2010C>G	XP_011517324.1:p.Asp670Glu
XM_011519023.3:c.1992C>G	XP_011517325.1:p.Asp664Glu
XM_011519029.3:c.435C>G	XP_011517331.1:p.Asp145Glu
XM_017015134.1:c.1989C>G	XP_016870623.1:p.Asp663Glu
XM_017015136.2:c.1905C>G	XP_016870625.1:p.Asp635Glu
XM_017015137.1:c.1890C>G	XP_016870626.1:p.Asp630Glu
XM_017015138.1:c.1890C>G	XP_016870627.1:p.Asp630Glu
XM_024447674.1:c.1833C>G	XP_024303442.1:p.Asp611Glu
XM_024447675.1:c.1767C>G	XP_024303443.1:p.Asp589Glu
XM_024447676.1:c.1128C>G	XP_024303444.1:p.Asp376Glu
XM_024447677.1:c.1128C>G	XP_024303445.1:p.Asp376Glu
XM_024447678.1:c.1911C>G	XP_024303446.1:p.Asp637Glu
XM_024447679.1:c.1911C>G	XP_024303447.1:p.Asp637Glu
XM_024447680.1:c.1746C>G	XP_024303448.1:p.Asp582Glu
NM_024757.5:c.2004C>G MANE Select	NP_079033.4:p.Asp668Glu
NM_001145527.2:c.2004C>G	NP_001138999.1:p.Asp668Glu
NM_001354259.2:c.1911C>G	NP_001341188.1:p.Asp637Glu
NM_001354263.2:c.1983C>G	NP_001341192.1:p.Asp661Glu