Canonical Allele Identifier: CA1884685674
Gene: EHMT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.137813020G= , CM000671.2:g.137813020G= GRCh38
NC_000009.11:g.140707472G= , CM000671.1:g.140707472G= GRCh37
NC_000009.10:g.139827293G= NCBI36
NG_011776.1:g.199029G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000460843.6:c.2882G= MANE Select ENSP00000417980.1:p.Arg961=
ENST00000636027.1:c.2768G= ENSP00000489961.1:p.Arg923=
ENST00000637161.1:c.2789G= ENSP00000490328.1:p.Arg930=
ENST00000637261.1:c.2922G= ENSP00000490815.1:n.2922G=
ENST00000637891.1:c.776G= ENSP00000490907.1:p.Arg259=
ENST00000460843.5:c.2882G= ENSP00000417980.1:p.Arg961=
ENST00000462942.3:c.1739G= ENSP00000436107.1:p.Arg580=
ENST00000486164.5:c.569G=
ENST00000488242.2:n.408G=
NM_024757.4:c.2882G= NP_079033.4:p.Arg961=
XM_005266105.3:c.2873G= XP_005266162.1:p.Arg958=
XM_005266110.1:c.2789G= XP_005266167.1:p.Arg930=
XM_006717288.2:c.2864G= XP_006717351.1:p.Arg955=
XM_011519021.1:c.2891G= XP_011517323.1:p.Arg964=
XM_011519022.1:c.2888G= XP_011517324.1:p.Arg963=
XM_011519023.1:c.2870G= XP_011517325.1:p.Arg957=
XM_011519024.1:c.2813G= XP_011517326.1:p.Arg938=
XM_011519025.1:c.2789G= XP_011517327.1:p.Arg930=
XM_011519026.1:c.2747G= XP_011517328.1:p.Arg916=
XM_011519029.1:c.1313G= XP_011517331.1:p.Arg438=
XM_011519030.1:c.665G= XP_011517332.1:p.Arg222=
XM_011519031.1:c.452G= XP_011517333.1:p.Arg151=
XM_011519032.1:c.452G= XP_011517334.1:p.Arg151=
XM_011519033.1:c.2726G= XP_011517335.1:p.Arg909=
NM_001354263.1:c.2861G= NP_001341192.1:p.Arg954=
XM_005266105.5:c.2873G= XP_005266162.1:p.Arg958=
XM_011519021.3:c.2891G= XP_011517323.1:p.Arg964=
XM_011519022.3:c.2888G= XP_011517324.1:p.Arg963=
XM_011519023.3:c.2870G= XP_011517325.1:p.Arg957=
XM_011519029.3:c.1313G= XP_011517331.1:p.Arg438=
XM_011519030.3:c.665G= XP_011517332.1:p.Arg222=
XM_017015134.1:c.2867G= XP_016870623.1:p.Arg956=
XM_017015136.2:c.2783G= XP_016870625.1:p.Arg928=
XM_017015137.1:c.2768G= XP_016870626.1:p.Arg923=
XM_017015138.1:c.2768G= XP_016870627.1:p.Arg923=
XM_024447674.1:c.2711G= XP_024303442.1:p.Arg904=
XM_024447675.1:c.2645G= XP_024303443.1:p.Arg882=
XM_024447676.1:c.2006G= XP_024303444.1:p.Arg669=
XM_024447677.1:c.2006G= XP_024303445.1:p.Arg669=
XM_024447680.1:c.2624G= XP_024303448.1:p.Arg875=
NM_024757.5:c.2882G= MANE Select NP_079033.4:p.Arg961=
NM_001354263.2:c.2861G= NP_001341192.1:p.Arg954=