Canonical Allele Identifier: CA1884685890
Gene: EHMT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.137813443C= , CM000671.2:g.137813443C= GRCh38
NC_000009.11:g.140707895C= , CM000671.1:g.140707895C= GRCh37
NC_000009.10:g.139827716C= NCBI36
NG_011776.1:g.199452C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000460843.6:c.3093C= MANE Select ENSP00000417980.1:p.Ser1031=
ENST00000637161.1:c.3000C= ENSP00000490328.1:p.Ser1000=
ENST00000637261.1:c.3133C= ENSP00000490815.1:n.3133C=
ENST00000637891.1:c.987C= ENSP00000490907.1:p.Ser329=
ENST00000460843.5:c.3093C= ENSP00000417980.1:p.Ser1031=
ENST00000462942.3:c.1950C= ENSP00000436107.1:p.Ser650=
ENST00000486164.5:c.780C=
ENST00000488242.2:n.619C=
NM_024757.4:c.3093C= NP_079033.4:p.Ser1031=
XM_005266105.3:c.3084C= XP_005266162.1:p.Ser1028=
XM_005266110.1:c.3000C= XP_005266167.1:p.Ser1000=
XM_006717288.2:c.3075C= XP_006717351.1:p.Ser1025=
XM_011519021.1:c.3102C= XP_011517323.1:p.Ser1034=
XM_011519022.1:c.3099C= XP_011517324.1:p.Ser1033=
XM_011519023.1:c.3081C= XP_011517325.1:p.Ser1027=
XM_011519024.1:c.3024C= XP_011517326.1:p.Ser1008=
XM_011519025.1:c.3000C= XP_011517327.1:p.Ser1000=
XM_011519026.1:c.2958C= XP_011517328.1:p.Ser986=
XM_011519029.1:c.1524C= XP_011517331.1:p.Ser508=
XM_011519030.1:c.876C= XP_011517332.1:p.Ser292=
XM_011519031.1:c.663C= XP_011517333.1:p.Ser221=
XM_011519032.1:c.663C= XP_011517334.1:p.Ser221=
XM_011519033.1:c.2937C= XP_011517335.1:p.Ser979=
NM_001354263.1:c.3072C= NP_001341192.1:p.Ser1024=
XM_005266105.5:c.3084C= XP_005266162.1:p.Ser1028=
XM_011519021.3:c.3102C= XP_011517323.1:p.Ser1034=
XM_011519022.3:c.3099C= XP_011517324.1:p.Ser1033=
XM_011519023.3:c.3081C= XP_011517325.1:p.Ser1027=
XM_011519029.3:c.1524C= XP_011517331.1:p.Ser508=
XM_011519030.3:c.876C= XP_011517332.1:p.Ser292=
XM_017015134.1:c.3078C= XP_016870623.1:p.Ser1026=
XM_017015136.2:c.2994C= XP_016870625.1:p.Ser998=
XM_017015137.1:c.2979C= XP_016870626.1:p.Ser993=
XM_017015138.1:c.2979C= XP_016870627.1:p.Ser993=
XM_024447674.1:c.2922C= XP_024303442.1:p.Ser974=
XM_024447675.1:c.2856C= XP_024303443.1:p.Ser952=
XM_024447676.1:c.2217C= XP_024303444.1:p.Ser739=
XM_024447677.1:c.2217C= XP_024303445.1:p.Ser739=
XM_024447680.1:c.2835C= XP_024303448.1:p.Ser945=
NM_024757.5:c.3093C= MANE Select NP_079033.4:p.Ser1031=
NM_001354263.2:c.3072C= NP_001341192.1:p.Ser1024=