Canonical Allele Identifier: CA468161398

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140707847T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137813395T>A , CM000671.2:g.137813395T>A	GRCh38
NC_000009.11:g.140707847T>A , CM000671.1:g.140707847T>A	GRCh37
NC_000009.10:g.139827668T>A	NCBI36
NG_011776.1:g.199404T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.3045T>A MANE Select	ENSP00000417980.1:p.Ala1015=
ENST00000636027.1:c.2931T>A	ENSP00000489961.1:p.Ala977=
ENST00000637161.1:c.2952T>A	ENSP00000490328.1:p.Ala984=
ENST00000637261.1:c.3085T>A	ENSP00000490815.1:n.3085T>A
ENST00000637891.1:c.939T>A	ENSP00000490907.1:p.Ala313=
ENST00000460843.5:c.3045T>A	ENSP00000417980.1:p.Ala1015=
ENST00000462942.3:c.1902T>A	ENSP00000436107.1:p.Ala634=
ENST00000486164.5:c.732T>A
ENST00000488242.2:n.571T>A
NM_024757.4:c.3045T>A	NP_079033.4:p.Ala1015=
XM_005266105.3:c.3036T>A	XP_005266162.1:p.Ala1012=
XM_005266110.1:c.2952T>A	XP_005266167.1:p.Ala984=
XM_006717288.2:c.3027T>A	XP_006717351.1:p.Ala1009=
XM_011519021.1:c.3054T>A	XP_011517323.1:p.Ala1018=
XM_011519022.1:c.3051T>A	XP_011517324.1:p.Ala1017=
XM_011519023.1:c.3033T>A	XP_011517325.1:p.Ala1011=
XM_011519024.1:c.2976T>A	XP_011517326.1:p.Ala992=
XM_011519025.1:c.2952T>A	XP_011517327.1:p.Ala984=
XM_011519026.1:c.2910T>A	XP_011517328.1:p.Ala970=
XM_011519029.1:c.1476T>A	XP_011517331.1:p.Ala492=
XM_011519030.1:c.828T>A	XP_011517332.1:p.Ala276=
XM_011519031.1:c.615T>A	XP_011517333.1:p.Ala205=
XM_011519032.1:c.615T>A	XP_011517334.1:p.Ala205=
XM_011519033.1:c.2889T>A	XP_011517335.1:p.Ala963=
NM_001354263.1:c.3024T>A	NP_001341192.1:p.Ala1008=
XM_005266105.5:c.3036T>A	XP_005266162.1:p.Ala1012=
XM_011519021.3:c.3054T>A	XP_011517323.1:p.Ala1018=
XM_011519022.3:c.3051T>A	XP_011517324.1:p.Ala1017=
XM_011519023.3:c.3033T>A	XP_011517325.1:p.Ala1011=
XM_011519029.3:c.1476T>A	XP_011517331.1:p.Ala492=
XM_011519030.3:c.828T>A	XP_011517332.1:p.Ala276=
XM_017015134.1:c.3030T>A	XP_016870623.1:p.Ala1010=
XM_017015136.2:c.2946T>A	XP_016870625.1:p.Ala982=
XM_017015137.1:c.2931T>A	XP_016870626.1:p.Ala977=
XM_017015138.1:c.2931T>A	XP_016870627.1:p.Ala977=
XM_024447674.1:c.2874T>A	XP_024303442.1:p.Ala958=
XM_024447675.1:c.2808T>A	XP_024303443.1:p.Ala936=
XM_024447676.1:c.2169T>A	XP_024303444.1:p.Ala723=
XM_024447677.1:c.2169T>A	XP_024303445.1:p.Ala723=
XM_024447680.1:c.2787T>A	XP_024303448.1:p.Ala929=
NM_024757.5:c.3045T>A MANE Select	NP_079033.4:p.Ala1015=
NM_001354263.2:c.3024T>A	NP_001341192.1:p.Ala1008=