Canonical Allele Identifier: CA467874118

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140671222C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137776770C>T , CM000671.2:g.137776770C>T	GRCh38
NC_000009.11:g.140671222C>T , CM000671.1:g.140671222C>T	GRCh37
NC_000009.10:g.139791043C>T	NCBI36
NG_011776.1:g.162779C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.1944C>T MANE Select	ENSP00000417980.1:p.Thr648=
ENST00000636027.1:c.1830C>T	ENSP00000489961.1:p.Thr610=
ENST00000637161.1:c.1851C>T	ENSP00000490328.1:p.Thr617=
ENST00000637261.1:c.1984C>T	ENSP00000490815.1:n.1984C>T
ENST00000638071.1:c.1571C>T
ENST00000640639.1:c.1113C>T	ENSP00000491823.1:p.Thr371=
ENST00000371394.6:c.*1679C>T	ENSP00000485945.1:n.*1679C>T
ENST00000460843.5:c.1944C>T	ENSP00000417980.1:p.Thr648=
ENST00000462484.5:c.1944C>T	ENSP00000417328.1:p.Thr648=
ENST00000462942.3:c.801C>T	ENSP00000436107.1:p.Thr267=
ENST00000465566.2:c.492C>T	ENSP00000486261.1:p.Thr164=
ENST00000626603.1:n.1679G>A
NM_001145527.1:c.1944C>T	NP_001138999.1:p.Thr648=
NM_024757.4:c.1944C>T	NP_079033.4:p.Thr648=
XM_005266105.3:c.1935C>T	XP_005266162.1:p.Thr645=
XM_005266110.1:c.1851C>T	XP_005266167.1:p.Thr617=
XM_006717288.2:c.1926C>T	XP_006717351.1:p.Thr642=
XM_011519021.1:c.1953C>T	XP_011517323.1:p.Thr651=
XM_011519022.1:c.1950C>T	XP_011517324.1:p.Thr650=
XM_011519023.1:c.1932C>T	XP_011517325.1:p.Thr644=
XM_011519024.1:c.1875C>T	XP_011517326.1:p.Thr625=
XM_011519025.1:c.1851C>T	XP_011517327.1:p.Thr617=
XM_011519026.1:c.1809C>T	XP_011517328.1:p.Thr603=
XM_011519027.1:c.1953C>T	XP_011517329.1:p.Thr651=
XM_011519028.1:c.1953C>T	XP_011517330.1:p.Thr651=
XM_011519029.1:c.375C>T	XP_011517331.1:p.Thr125=
XM_011519033.1:c.1788C>T	XP_011517335.1:p.Thr596=
NM_001354259.1:c.1851C>T	NP_001341188.1:p.Thr617=
NM_001354263.1:c.1923C>T	NP_001341192.1:p.Thr641=
XM_005266105.5:c.1935C>T	XP_005266162.1:p.Thr645=
XM_011519021.3:c.1953C>T	XP_011517323.1:p.Thr651=
XM_011519022.3:c.1950C>T	XP_011517324.1:p.Thr650=
XM_011519023.3:c.1932C>T	XP_011517325.1:p.Thr644=
XM_011519029.3:c.375C>T	XP_011517331.1:p.Thr125=
XM_017015134.1:c.1929C>T	XP_016870623.1:p.Thr643=
XM_017015136.2:c.1845C>T	XP_016870625.1:p.Thr615=
XM_017015137.1:c.1830C>T	XP_016870626.1:p.Thr610=
XM_017015138.1:c.1830C>T	XP_016870627.1:p.Thr610=
XM_024447674.1:c.1773C>T	XP_024303442.1:p.Thr591=
XM_024447675.1:c.1707C>T	XP_024303443.1:p.Thr569=
XM_024447676.1:c.1068C>T	XP_024303444.1:p.Thr356=
XM_024447677.1:c.1068C>T	XP_024303445.1:p.Thr356=
XM_024447678.1:c.1851C>T	XP_024303446.1:p.Thr617=
XM_024447679.1:c.1851C>T	XP_024303447.1:p.Thr617=
XM_024447680.1:c.1686C>T	XP_024303448.1:p.Thr562=
NM_024757.5:c.1944C>T MANE Select	NP_079033.4:p.Thr648=
NM_001145527.2:c.1944C>T	NP_001138999.1:p.Thr648=
NM_001354259.2:c.1851C>T	NP_001341188.1:p.Thr617=
NM_001354263.2:c.1923C>T	NP_001341192.1:p.Thr641=