Canonical Allele Identifier: CA1884679275
Gene: EHMT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.137800924G= , CM000671.2:g.137800924G= GRCh38
NC_000009.11:g.140695376G= , CM000671.1:g.140695376G= GRCh37
NC_000009.10:g.139815197G= NCBI36
NG_011776.1:g.186933G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000460843.6:c.2652G= MANE Select ENSP00000417980.1:p.Lys884=
ENST00000636027.1:c.2538G= ENSP00000489961.1:p.Lys846=
ENST00000637161.1:c.2559G= ENSP00000490328.1:p.Lys853=
ENST00000637261.1:c.2692G= ENSP00000490815.1:n.2692G=
ENST00000637891.1:c.546G= ENSP00000490907.1:p.Lys182=
ENST00000637949.1:c.330G= ENSP00000489786.1:p.Lys110=
ENST00000460843.5:c.2652G= ENSP00000417980.1:p.Lys884=
ENST00000462942.3:c.1509G= ENSP00000436107.1:p.Lys503=
ENST00000482340.5:c.222G= ENSP00000486748.1:p.Lys74=
ENST00000486164.5:c.230G=
ENST00000488242.2:n.178G=
ENST00000493484.5:c.222G= ENSP00000486503.1:p.Lys74=
NM_024757.4:c.2652G= NP_079033.4:p.Lys884=
XM_005266105.3:c.2643G= XP_005266162.1:p.Lys881=
XM_005266110.1:c.2559G= XP_005266167.1:p.Lys853=
XM_006717288.2:c.2634G= XP_006717351.1:p.Lys878=
XM_011519021.1:c.2661G= XP_011517323.1:p.Lys887=
XM_011519022.1:c.2658G= XP_011517324.1:p.Lys886=
XM_011519023.1:c.2640G= XP_011517325.1:p.Lys880=
XM_011519024.1:c.2583G= XP_011517326.1:p.Lys861=
XM_011519025.1:c.2559G= XP_011517327.1:p.Lys853=
XM_011519026.1:c.2517G= XP_011517328.1:p.Lys839=
XM_011519027.1:c.2661G= XP_011517329.1:p.Lys887=
XM_011519029.1:c.1083G= XP_011517331.1:p.Lys361=
XM_011519030.1:c.435G= XP_011517332.1:p.Lys145=
XM_011519031.1:c.222G= XP_011517333.1:p.Lys74=
XM_011519032.1:c.222G= XP_011517334.1:p.Lys74=
XM_011519033.1:c.2496G= XP_011517335.1:p.Lys832=
NM_001354263.1:c.2631G= NP_001341192.1:p.Lys877=
XM_005266105.5:c.2643G= XP_005266162.1:p.Lys881=
XM_011519021.3:c.2661G= XP_011517323.1:p.Lys887=
XM_011519022.3:c.2658G= XP_011517324.1:p.Lys886=
XM_011519023.3:c.2640G= XP_011517325.1:p.Lys880=
XM_011519029.3:c.1083G= XP_011517331.1:p.Lys361=
XM_011519030.3:c.435G= XP_011517332.1:p.Lys145=
XM_017015134.1:c.2637G= XP_016870623.1:p.Lys879=
XM_017015136.2:c.2553G= XP_016870625.1:p.Lys851=
XM_017015137.1:c.2538G= XP_016870626.1:p.Lys846=
XM_017015138.1:c.2538G= XP_016870627.1:p.Lys846=
XM_024447674.1:c.2481G= XP_024303442.1:p.Lys827=
XM_024447675.1:c.2415G= XP_024303443.1:p.Lys805=
XM_024447676.1:c.1776G= XP_024303444.1:p.Lys592=
XM_024447677.1:c.1776G= XP_024303445.1:p.Lys592=
XM_024447678.1:c.2559G= XP_024303446.1:p.Lys853=
XM_024447680.1:c.2394G= XP_024303448.1:p.Lys798=
NM_024757.5:c.2652G= MANE Select NP_079033.4:p.Lys884=
NM_001354263.2:c.2631G= NP_001341192.1:p.Lys877=