Canonical Allele Identifier: CA1884685691
Gene: EHMT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.137813079C= , CM000671.2:g.137813079C= GRCh38
NC_000009.11:g.140707531C= , CM000671.1:g.140707531C= GRCh37
NC_000009.10:g.139827352C= NCBI36
NG_011776.1:g.199088C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000460843.6:c.2941C= MANE Select ENSP00000417980.1:p.Leu981=
ENST00000636027.1:c.2827C= ENSP00000489961.1:p.Leu943=
ENST00000637161.1:c.2848C= ENSP00000490328.1:p.Leu950=
ENST00000637261.1:c.2981C= ENSP00000490815.1:n.2981C=
ENST00000637891.1:c.835C= ENSP00000490907.1:p.Leu279=
ENST00000460843.5:c.2941C= ENSP00000417980.1:p.Leu981=
ENST00000462942.3:c.1798C= ENSP00000436107.1:p.Leu600=
ENST00000486164.5:c.628C=
ENST00000488242.2:n.467C=
NM_024757.4:c.2941C= NP_079033.4:p.Leu981=
XM_005266105.3:c.2932C= XP_005266162.1:p.Leu978=
XM_005266110.1:c.2848C= XP_005266167.1:p.Leu950=
XM_006717288.2:c.2923C= XP_006717351.1:p.Leu975=
XM_011519021.1:c.2950C= XP_011517323.1:p.Leu984=
XM_011519022.1:c.2947C= XP_011517324.1:p.Leu983=
XM_011519023.1:c.2929C= XP_011517325.1:p.Leu977=
XM_011519024.1:c.2872C= XP_011517326.1:p.Leu958=
XM_011519025.1:c.2848C= XP_011517327.1:p.Leu950=
XM_011519026.1:c.2806C= XP_011517328.1:p.Leu936=
XM_011519029.1:c.1372C= XP_011517331.1:p.Leu458=
XM_011519030.1:c.724C= XP_011517332.1:p.Leu242=
XM_011519031.1:c.511C= XP_011517333.1:p.Leu171=
XM_011519032.1:c.511C= XP_011517334.1:p.Leu171=
XM_011519033.1:c.2785C= XP_011517335.1:p.Leu929=
NM_001354263.1:c.2920C= NP_001341192.1:p.Leu974=
XM_005266105.5:c.2932C= XP_005266162.1:p.Leu978=
XM_011519021.3:c.2950C= XP_011517323.1:p.Leu984=
XM_011519022.3:c.2947C= XP_011517324.1:p.Leu983=
XM_011519023.3:c.2929C= XP_011517325.1:p.Leu977=
XM_011519029.3:c.1372C= XP_011517331.1:p.Leu458=
XM_011519030.3:c.724C= XP_011517332.1:p.Leu242=
XM_017015134.1:c.2926C= XP_016870623.1:p.Leu976=
XM_017015136.2:c.2842C= XP_016870625.1:p.Leu948=
XM_017015137.1:c.2827C= XP_016870626.1:p.Leu943=
XM_017015138.1:c.2827C= XP_016870627.1:p.Leu943=
XM_024447674.1:c.2770C= XP_024303442.1:p.Leu924=
XM_024447675.1:c.2704C= XP_024303443.1:p.Leu902=
XM_024447676.1:c.2065C= XP_024303444.1:p.Leu689=
XM_024447677.1:c.2065C= XP_024303445.1:p.Leu689=
XM_024447680.1:c.2683C= XP_024303448.1:p.Leu895=
NM_024757.5:c.2941C= MANE Select NP_079033.4:p.Leu981=
NM_001354263.2:c.2920C= NP_001341192.1:p.Leu974=