Canonical Allele Identifier: CA467874170

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140671294C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137776842C>G , CM000671.2:g.137776842C>G	GRCh38
NC_000009.11:g.140671294C>G , CM000671.1:g.140671294C>G	GRCh37
NC_000009.10:g.139791115C>G	NCBI36
NG_011776.1:g.162851C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.2016C>G MANE Select	ENSP00000417980.1:p.Gly672=
ENST00000636027.1:c.1902C>G	ENSP00000489961.1:p.Gly634=
ENST00000637161.1:c.1923C>G	ENSP00000490328.1:p.Gly641=
ENST00000637261.1:c.2056C>G	ENSP00000490815.1:n.2056C>G
ENST00000638071.1:c.1643C>G
ENST00000371394.6:c.*1751C>G	ENSP00000485945.1:n.*1751C>G
ENST00000460843.5:c.2016C>G	ENSP00000417980.1:p.Gly672=
ENST00000462484.5:c.2016C>G	ENSP00000417328.1:p.Gly672=
ENST00000462942.3:c.873C>G	ENSP00000436107.1:p.Gly291=
ENST00000626603.1:n.1607G>C
NM_001145527.1:c.2016C>G	NP_001138999.1:p.Gly672=
NM_024757.4:c.2016C>G	NP_079033.4:p.Gly672=
XM_005266105.3:c.2007C>G	XP_005266162.1:p.Gly669=
XM_005266110.1:c.1923C>G	XP_005266167.1:p.Gly641=
XM_006717288.2:c.1998C>G	XP_006717351.1:p.Gly666=
XM_011519021.1:c.2025C>G	XP_011517323.1:p.Gly675=
XM_011519022.1:c.2022C>G	XP_011517324.1:p.Gly674=
XM_011519023.1:c.2004C>G	XP_011517325.1:p.Gly668=
XM_011519024.1:c.1947C>G	XP_011517326.1:p.Gly649=
XM_011519025.1:c.1923C>G	XP_011517327.1:p.Gly641=
XM_011519026.1:c.1881C>G	XP_011517328.1:p.Gly627=
XM_011519027.1:c.2025C>G	XP_011517329.1:p.Gly675=
XM_011519028.1:c.2025C>G	XP_011517330.1:p.Gly675=
XM_011519029.1:c.447C>G	XP_011517331.1:p.Gly149=
XM_011519033.1:c.1860C>G	XP_011517335.1:p.Gly620=
NM_001354259.1:c.1923C>G	NP_001341188.1:p.Gly641=
NM_001354263.1:c.1995C>G	NP_001341192.1:p.Gly665=
XM_005266105.5:c.2007C>G	XP_005266162.1:p.Gly669=
XM_011519021.3:c.2025C>G	XP_011517323.1:p.Gly675=
XM_011519022.3:c.2022C>G	XP_011517324.1:p.Gly674=
XM_011519023.3:c.2004C>G	XP_011517325.1:p.Gly668=
XM_011519029.3:c.447C>G	XP_011517331.1:p.Gly149=
XM_017015134.1:c.2001C>G	XP_016870623.1:p.Gly667=
XM_017015136.2:c.1917C>G	XP_016870625.1:p.Gly639=
XM_017015137.1:c.1902C>G	XP_016870626.1:p.Gly634=
XM_017015138.1:c.1902C>G	XP_016870627.1:p.Gly634=
XM_024447674.1:c.1845C>G	XP_024303442.1:p.Gly615=
XM_024447675.1:c.1779C>G	XP_024303443.1:p.Gly593=
XM_024447676.1:c.1140C>G	XP_024303444.1:p.Gly380=
XM_024447677.1:c.1140C>G	XP_024303445.1:p.Gly380=
XM_024447678.1:c.1923C>G	XP_024303446.1:p.Gly641=
XM_024447679.1:c.1923C>G	XP_024303447.1:p.Gly641=
XM_024447680.1:c.1758C>G	XP_024303448.1:p.Gly586=
NM_024757.5:c.2016C>G MANE Select	NP_079033.4:p.Gly672=
NM_001145527.2:c.2016C>G	NP_001138999.1:p.Gly672=
NM_001354259.2:c.1923C>G	NP_001341188.1:p.Gly641=
NM_001354263.2:c.1995C>G	NP_001341192.1:p.Gly665=