Canonical Allele Identifier: CA1884685697
Gene: EHMT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.137813090G= , CM000671.2:g.137813090G= GRCh38
NC_000009.11:g.140707542G= , CM000671.1:g.140707542G= GRCh37
NC_000009.10:g.139827363G= NCBI36
NG_011776.1:g.199099G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000460843.6:c.2952G= MANE Select ENSP00000417980.1:p.Gln984=
ENST00000636027.1:c.2838G= ENSP00000489961.1:p.Gln946=
ENST00000637161.1:c.2859G= ENSP00000490328.1:p.Gln953=
ENST00000637261.1:c.2992G= ENSP00000490815.1:n.2992G=
ENST00000637891.1:c.846G= ENSP00000490907.1:p.Gln282=
ENST00000460843.5:c.2952G= ENSP00000417980.1:p.Gln984=
ENST00000462942.3:c.1809G= ENSP00000436107.1:p.Gln603=
ENST00000486164.5:c.639G=
ENST00000488242.2:n.478G=
NM_024757.4:c.2952G= NP_079033.4:p.Gln984=
XM_005266105.3:c.2943G= XP_005266162.1:p.Gln981=
XM_005266110.1:c.2859G= XP_005266167.1:p.Gln953=
XM_006717288.2:c.2934G= XP_006717351.1:p.Gln978=
XM_011519021.1:c.2961G= XP_011517323.1:p.Gln987=
XM_011519022.1:c.2958G= XP_011517324.1:p.Gln986=
XM_011519023.1:c.2940G= XP_011517325.1:p.Gln980=
XM_011519024.1:c.2883G= XP_011517326.1:p.Gln961=
XM_011519025.1:c.2859G= XP_011517327.1:p.Gln953=
XM_011519026.1:c.2817G= XP_011517328.1:p.Gln939=
XM_011519029.1:c.1383G= XP_011517331.1:p.Gln461=
XM_011519030.1:c.735G= XP_011517332.1:p.Gln245=
XM_011519031.1:c.522G= XP_011517333.1:p.Gln174=
XM_011519032.1:c.522G= XP_011517334.1:p.Gln174=
XM_011519033.1:c.2796G= XP_011517335.1:p.Gln932=
NM_001354263.1:c.2931G= NP_001341192.1:p.Gln977=
XM_005266105.5:c.2943G= XP_005266162.1:p.Gln981=
XM_011519021.3:c.2961G= XP_011517323.1:p.Gln987=
XM_011519022.3:c.2958G= XP_011517324.1:p.Gln986=
XM_011519023.3:c.2940G= XP_011517325.1:p.Gln980=
XM_011519029.3:c.1383G= XP_011517331.1:p.Gln461=
XM_011519030.3:c.735G= XP_011517332.1:p.Gln245=
XM_017015134.1:c.2937G= XP_016870623.1:p.Gln979=
XM_017015136.2:c.2853G= XP_016870625.1:p.Gln951=
XM_017015137.1:c.2838G= XP_016870626.1:p.Gln946=
XM_017015138.1:c.2838G= XP_016870627.1:p.Gln946=
XM_024447674.1:c.2781G= XP_024303442.1:p.Gln927=
XM_024447675.1:c.2715G= XP_024303443.1:p.Gln905=
XM_024447676.1:c.2076G= XP_024303444.1:p.Gln692=
XM_024447677.1:c.2076G= XP_024303445.1:p.Gln692=
XM_024447680.1:c.2694G= XP_024303448.1:p.Gln898=
NM_024757.5:c.2952G= MANE Select NP_079033.4:p.Gln984=
NM_001354263.2:c.2931G= NP_001341192.1:p.Gln977=