Canonical Allele Identifier: CA468161044

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140707506A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137813054A>T , CM000671.2:g.137813054A>T	GRCh38
NC_000009.11:g.140707506A>T , CM000671.1:g.140707506A>T	GRCh37
NC_000009.10:g.139827327A>T	NCBI36
NG_011776.1:g.199063A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.2916A>T MANE Select	ENSP00000417980.1:p.Gly972=
ENST00000636027.1:c.2802A>T	ENSP00000489961.1:p.Gly934=
ENST00000637161.1:c.2823A>T	ENSP00000490328.1:p.Gly941=
ENST00000637261.1:c.2956A>T	ENSP00000490815.1:n.2956A>T
ENST00000637891.1:c.810A>T	ENSP00000490907.1:p.Gly270=
ENST00000460843.5:c.2916A>T	ENSP00000417980.1:p.Gly972=
ENST00000462942.3:c.1773A>T	ENSP00000436107.1:p.Gly591=
ENST00000486164.5:c.603A>T
ENST00000488242.2:n.442A>T
NM_024757.4:c.2916A>T	NP_079033.4:p.Gly972=
XM_005266105.3:c.2907A>T	XP_005266162.1:p.Gly969=
XM_005266110.1:c.2823A>T	XP_005266167.1:p.Gly941=
XM_006717288.2:c.2898A>T	XP_006717351.1:p.Gly966=
XM_011519021.1:c.2925A>T	XP_011517323.1:p.Gly975=
XM_011519022.1:c.2922A>T	XP_011517324.1:p.Gly974=
XM_011519023.1:c.2904A>T	XP_011517325.1:p.Gly968=
XM_011519024.1:c.2847A>T	XP_011517326.1:p.Gly949=
XM_011519025.1:c.2823A>T	XP_011517327.1:p.Gly941=
XM_011519026.1:c.2781A>T	XP_011517328.1:p.Gly927=
XM_011519029.1:c.1347A>T	XP_011517331.1:p.Gly449=
XM_011519030.1:c.699A>T	XP_011517332.1:p.Gly233=
XM_011519031.1:c.486A>T	XP_011517333.1:p.Gly162=
XM_011519032.1:c.486A>T	XP_011517334.1:p.Gly162=
XM_011519033.1:c.2760A>T	XP_011517335.1:p.Gly920=
NM_001354263.1:c.2895A>T	NP_001341192.1:p.Gly965=
XM_005266105.5:c.2907A>T	XP_005266162.1:p.Gly969=
XM_011519021.3:c.2925A>T	XP_011517323.1:p.Gly975=
XM_011519022.3:c.2922A>T	XP_011517324.1:p.Gly974=
XM_011519023.3:c.2904A>T	XP_011517325.1:p.Gly968=
XM_011519029.3:c.1347A>T	XP_011517331.1:p.Gly449=
XM_011519030.3:c.699A>T	XP_011517332.1:p.Gly233=
XM_017015134.1:c.2901A>T	XP_016870623.1:p.Gly967=
XM_017015136.2:c.2817A>T	XP_016870625.1:p.Gly939=
XM_017015137.1:c.2802A>T	XP_016870626.1:p.Gly934=
XM_017015138.1:c.2802A>T	XP_016870627.1:p.Gly934=
XM_024447674.1:c.2745A>T	XP_024303442.1:p.Gly915=
XM_024447675.1:c.2679A>T	XP_024303443.1:p.Gly893=
XM_024447676.1:c.2040A>T	XP_024303444.1:p.Gly680=
XM_024447677.1:c.2040A>T	XP_024303445.1:p.Gly680=
XM_024447680.1:c.2658A>T	XP_024303448.1:p.Gly886=
NM_024757.5:c.2916A>T MANE Select	NP_079033.4:p.Gly972=
NM_001354263.2:c.2895A>T	NP_001341192.1:p.Gly965=