Canonical Allele Identifier: CA1884685681
Gene: EHMT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.137813047A= , CM000671.2:g.137813047A= GRCh38
NC_000009.11:g.140707499A= , CM000671.1:g.140707499A= GRCh37
NC_000009.10:g.139827320A= NCBI36
NG_011776.1:g.199056A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000460843.6:c.2909A= MANE Select ENSP00000417980.1:p.Lys970=
ENST00000636027.1:c.2795A= ENSP00000489961.1:p.Lys932=
ENST00000637161.1:c.2816A= ENSP00000490328.1:p.Lys939=
ENST00000637261.1:c.2949A= ENSP00000490815.1:n.2949A=
ENST00000637891.1:c.803A= ENSP00000490907.1:p.Lys268=
ENST00000460843.5:c.2909A= ENSP00000417980.1:p.Lys970=
ENST00000462942.3:c.1766A= ENSP00000436107.1:p.Lys589=
ENST00000486164.5:c.596A=
ENST00000488242.2:n.435A=
NM_024757.4:c.2909A= NP_079033.4:p.Lys970=
XM_005266105.3:c.2900A= XP_005266162.1:p.Lys967=
XM_005266110.1:c.2816A= XP_005266167.1:p.Lys939=
XM_006717288.2:c.2891A= XP_006717351.1:p.Lys964=
XM_011519021.1:c.2918A= XP_011517323.1:p.Lys973=
XM_011519022.1:c.2915A= XP_011517324.1:p.Lys972=
XM_011519023.1:c.2897A= XP_011517325.1:p.Lys966=
XM_011519024.1:c.2840A= XP_011517326.1:p.Lys947=
XM_011519025.1:c.2816A= XP_011517327.1:p.Lys939=
XM_011519026.1:c.2774A= XP_011517328.1:p.Lys925=
XM_011519029.1:c.1340A= XP_011517331.1:p.Lys447=
XM_011519030.1:c.692A= XP_011517332.1:p.Lys231=
XM_011519031.1:c.479A= XP_011517333.1:p.Lys160=
XM_011519032.1:c.479A= XP_011517334.1:p.Lys160=
XM_011519033.1:c.2753A= XP_011517335.1:p.Lys918=
NM_001354263.1:c.2888A= NP_001341192.1:p.Lys963=
XM_005266105.5:c.2900A= XP_005266162.1:p.Lys967=
XM_011519021.3:c.2918A= XP_011517323.1:p.Lys973=
XM_011519022.3:c.2915A= XP_011517324.1:p.Lys972=
XM_011519023.3:c.2897A= XP_011517325.1:p.Lys966=
XM_011519029.3:c.1340A= XP_011517331.1:p.Lys447=
XM_011519030.3:c.692A= XP_011517332.1:p.Lys231=
XM_017015134.1:c.2894A= XP_016870623.1:p.Lys965=
XM_017015136.2:c.2810A= XP_016870625.1:p.Lys937=
XM_017015137.1:c.2795A= XP_016870626.1:p.Lys932=
XM_017015138.1:c.2795A= XP_016870627.1:p.Lys932=
XM_024447674.1:c.2738A= XP_024303442.1:p.Lys913=
XM_024447675.1:c.2672A= XP_024303443.1:p.Lys891=
XM_024447676.1:c.2033A= XP_024303444.1:p.Lys678=
XM_024447677.1:c.2033A= XP_024303445.1:p.Lys678=
XM_024447680.1:c.2651A= XP_024303448.1:p.Lys884=
NM_024757.5:c.2909A= MANE Select NP_079033.4:p.Lys970=
NM_001354263.2:c.2888A= NP_001341192.1:p.Lys963=