Canonical Allele Identifier: CA1884685679
Gene: EHMT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.137813042G= , CM000671.2:g.137813042G= GRCh38
NC_000009.11:g.140707494G= , CM000671.1:g.140707494G= GRCh37
NC_000009.10:g.139827315G= NCBI36
NG_011776.1:g.199051G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000460843.6:c.2904G= MANE Select ENSP00000417980.1:p.Lys968=
ENST00000636027.1:c.2790G= ENSP00000489961.1:p.Lys930=
ENST00000637161.1:c.2811G= ENSP00000490328.1:p.Lys937=
ENST00000637261.1:c.2944G= ENSP00000490815.1:n.2944G=
ENST00000637891.1:c.798G= ENSP00000490907.1:p.Lys266=
ENST00000460843.5:c.2904G= ENSP00000417980.1:p.Lys968=
ENST00000462942.3:c.1761G= ENSP00000436107.1:p.Lys587=
ENST00000486164.5:c.591G=
ENST00000488242.2:n.430G=
NM_024757.4:c.2904G= NP_079033.4:p.Lys968=
XM_005266105.3:c.2895G= XP_005266162.1:p.Lys965=
XM_005266110.1:c.2811G= XP_005266167.1:p.Lys937=
XM_006717288.2:c.2886G= XP_006717351.1:p.Lys962=
XM_011519021.1:c.2913G= XP_011517323.1:p.Lys971=
XM_011519022.1:c.2910G= XP_011517324.1:p.Lys970=
XM_011519023.1:c.2892G= XP_011517325.1:p.Lys964=
XM_011519024.1:c.2835G= XP_011517326.1:p.Lys945=
XM_011519025.1:c.2811G= XP_011517327.1:p.Lys937=
XM_011519026.1:c.2769G= XP_011517328.1:p.Lys923=
XM_011519029.1:c.1335G= XP_011517331.1:p.Lys445=
XM_011519030.1:c.687G= XP_011517332.1:p.Lys229=
XM_011519031.1:c.474G= XP_011517333.1:p.Lys158=
XM_011519032.1:c.474G= XP_011517334.1:p.Lys158=
XM_011519033.1:c.2748G= XP_011517335.1:p.Lys916=
NM_001354263.1:c.2883G= NP_001341192.1:p.Lys961=
XM_005266105.5:c.2895G= XP_005266162.1:p.Lys965=
XM_011519021.3:c.2913G= XP_011517323.1:p.Lys971=
XM_011519022.3:c.2910G= XP_011517324.1:p.Lys970=
XM_011519023.3:c.2892G= XP_011517325.1:p.Lys964=
XM_011519029.3:c.1335G= XP_011517331.1:p.Lys445=
XM_011519030.3:c.687G= XP_011517332.1:p.Lys229=
XM_017015134.1:c.2889G= XP_016870623.1:p.Lys963=
XM_017015136.2:c.2805G= XP_016870625.1:p.Lys935=
XM_017015137.1:c.2790G= XP_016870626.1:p.Lys930=
XM_017015138.1:c.2790G= XP_016870627.1:p.Lys930=
XM_024447674.1:c.2733G= XP_024303442.1:p.Lys911=
XM_024447675.1:c.2667G= XP_024303443.1:p.Lys889=
XM_024447676.1:c.2028G= XP_024303444.1:p.Lys676=
XM_024447677.1:c.2028G= XP_024303445.1:p.Lys676=
XM_024447680.1:c.2646G= XP_024303448.1:p.Lys882=
NM_024757.5:c.2904G= MANE Select NP_079033.4:p.Lys968=
NM_001354263.2:c.2883G= NP_001341192.1:p.Lys961=