Canonical Allele Identifier: CA1884685683
Gene: EHMT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.137813059C= , CM000671.2:g.137813059C= GRCh38
NC_000009.11:g.140707511C= , CM000671.1:g.140707511C= GRCh37
NC_000009.10:g.139827332C= NCBI36
NG_011776.1:g.199068C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000460843.6:c.2921C= MANE Select ENSP00000417980.1:p.Thr974=
ENST00000636027.1:c.2807C= ENSP00000489961.1:p.Thr936=
ENST00000637161.1:c.2828C= ENSP00000490328.1:p.Thr943=
ENST00000637261.1:c.2961C= ENSP00000490815.1:n.2961C=
ENST00000637891.1:c.815C= ENSP00000490907.1:p.Thr272=
ENST00000460843.5:c.2921C= ENSP00000417980.1:p.Thr974=
ENST00000462942.3:c.1778C= ENSP00000436107.1:p.Thr593=
ENST00000486164.5:c.608C=
ENST00000488242.2:n.447C=
NM_024757.4:c.2921C= NP_079033.4:p.Thr974=
XM_005266105.3:c.2912C= XP_005266162.1:p.Thr971=
XM_005266110.1:c.2828C= XP_005266167.1:p.Thr943=
XM_006717288.2:c.2903C= XP_006717351.1:p.Thr968=
XM_011519021.1:c.2930C= XP_011517323.1:p.Thr977=
XM_011519022.1:c.2927C= XP_011517324.1:p.Thr976=
XM_011519023.1:c.2909C= XP_011517325.1:p.Thr970=
XM_011519024.1:c.2852C= XP_011517326.1:p.Thr951=
XM_011519025.1:c.2828C= XP_011517327.1:p.Thr943=
XM_011519026.1:c.2786C= XP_011517328.1:p.Thr929=
XM_011519029.1:c.1352C= XP_011517331.1:p.Thr451=
XM_011519030.1:c.704C= XP_011517332.1:p.Thr235=
XM_011519031.1:c.491C= XP_011517333.1:p.Thr164=
XM_011519032.1:c.491C= XP_011517334.1:p.Thr164=
XM_011519033.1:c.2765C= XP_011517335.1:p.Thr922=
NM_001354263.1:c.2900C= NP_001341192.1:p.Thr967=
XM_005266105.5:c.2912C= XP_005266162.1:p.Thr971=
XM_011519021.3:c.2930C= XP_011517323.1:p.Thr977=
XM_011519022.3:c.2927C= XP_011517324.1:p.Thr976=
XM_011519023.3:c.2909C= XP_011517325.1:p.Thr970=
XM_011519029.3:c.1352C= XP_011517331.1:p.Thr451=
XM_011519030.3:c.704C= XP_011517332.1:p.Thr235=
XM_017015134.1:c.2906C= XP_016870623.1:p.Thr969=
XM_017015136.2:c.2822C= XP_016870625.1:p.Thr941=
XM_017015137.1:c.2807C= XP_016870626.1:p.Thr936=
XM_017015138.1:c.2807C= XP_016870627.1:p.Thr936=
XM_024447674.1:c.2750C= XP_024303442.1:p.Thr917=
XM_024447675.1:c.2684C= XP_024303443.1:p.Thr895=
XM_024447676.1:c.2045C= XP_024303444.1:p.Thr682=
XM_024447677.1:c.2045C= XP_024303445.1:p.Thr682=
XM_024447680.1:c.2663C= XP_024303448.1:p.Thr888=
NM_024757.5:c.2921C= MANE Select NP_079033.4:p.Thr974=
NM_001354263.2:c.2900C= NP_001341192.1:p.Thr967=