Canonical Allele Identifier: CA1884685709
Gene: EHMT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.137813109A= , CM000671.2:g.137813109A= GRCh38
NC_000009.11:g.140707561A= , CM000671.1:g.140707561A= GRCh37
NC_000009.10:g.139827382A= NCBI36
NG_011776.1:g.199118A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000460843.6:c.2971A= MANE Select ENSP00000417980.1:p.Met991=
ENST00000636027.1:c.2857A= ENSP00000489961.1:p.Met953=
ENST00000637161.1:c.2878A= ENSP00000490328.1:p.Met960=
ENST00000637261.1:c.3011A= ENSP00000490815.1:n.3011A=
ENST00000637891.1:c.865A= ENSP00000490907.1:p.Met289=
ENST00000460843.5:c.2971A= ENSP00000417980.1:p.Met991=
ENST00000462942.3:c.1828A= ENSP00000436107.1:p.Met610=
ENST00000486164.5:c.658A=
ENST00000488242.2:n.497A=
NM_024757.4:c.2971A= NP_079033.4:p.Met991=
XM_005266105.3:c.2962A= XP_005266162.1:p.Met988=
XM_005266110.1:c.2878A= XP_005266167.1:p.Met960=
XM_006717288.2:c.2953A= XP_006717351.1:p.Met985=
XM_011519021.1:c.2980A= XP_011517323.1:p.Met994=
XM_011519022.1:c.2977A= XP_011517324.1:p.Met993=
XM_011519023.1:c.2959A= XP_011517325.1:p.Met987=
XM_011519024.1:c.2902A= XP_011517326.1:p.Met968=
XM_011519025.1:c.2878A= XP_011517327.1:p.Met960=
XM_011519026.1:c.2836A= XP_011517328.1:p.Met946=
XM_011519029.1:c.1402A= XP_011517331.1:p.Met468=
XM_011519030.1:c.754A= XP_011517332.1:p.Met252=
XM_011519031.1:c.541A= XP_011517333.1:p.Met181=
XM_011519032.1:c.541A= XP_011517334.1:p.Met181=
XM_011519033.1:c.2815A= XP_011517335.1:p.Met939=
NM_001354263.1:c.2950A= NP_001341192.1:p.Met984=
XM_005266105.5:c.2962A= XP_005266162.1:p.Met988=
XM_011519021.3:c.2980A= XP_011517323.1:p.Met994=
XM_011519022.3:c.2977A= XP_011517324.1:p.Met993=
XM_011519023.3:c.2959A= XP_011517325.1:p.Met987=
XM_011519029.3:c.1402A= XP_011517331.1:p.Met468=
XM_011519030.3:c.754A= XP_011517332.1:p.Met252=
XM_017015134.1:c.2956A= XP_016870623.1:p.Met986=
XM_017015136.2:c.2872A= XP_016870625.1:p.Met958=
XM_017015137.1:c.2857A= XP_016870626.1:p.Met953=
XM_017015138.1:c.2857A= XP_016870627.1:p.Met953=
XM_024447674.1:c.2800A= XP_024303442.1:p.Met934=
XM_024447675.1:c.2734A= XP_024303443.1:p.Met912=
XM_024447676.1:c.2095A= XP_024303444.1:p.Met699=
XM_024447677.1:c.2095A= XP_024303445.1:p.Met699=
XM_024447680.1:c.2713A= XP_024303448.1:p.Met905=
NM_024757.5:c.2971A= MANE Select NP_079033.4:p.Met991=
NM_001354263.2:c.2950A= NP_001341192.1:p.Met984=