Canonical Allele Identifier: CA1884688366
Gene: EHMT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.137818099T= , CM000671.2:g.137818099T= GRCh38
NC_000009.11:g.140712551T= , CM000671.1:g.140712551T= GRCh37
NC_000009.10:g.139832372T= NCBI36
NG_011776.1:g.204108T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000460843.6:c.3501T= MANE Select ENSP00000417980.1:p.Val1167=
ENST00000636472.1:n.63T=
ENST00000637161.1:c.3408T= ENSP00000490328.1:p.Val1136=
ENST00000637261.1:c.4075T= ENSP00000490815.1:n.4075T=
ENST00000637748.1:n.482T=
ENST00000637891.1:c.1575T= ENSP00000490907.1:n.1575T=
ENST00000460843.5:c.3501T= ENSP00000417980.1:p.Val1167=
ENST00000462942.3:c.2358T= ENSP00000436107.1:p.Val786=
ENST00000475564.5:n.1225T=
ENST00000494249.5:n.854T=
NM_024757.4:c.3501T= NP_079033.4:p.Val1167=
XM_005266105.3:c.3492T= XP_005266162.1:p.Val1164=
XM_005266110.1:c.3408T= XP_005266167.1:p.Val1136=
XM_006717288.2:c.3483T= XP_006717351.1:p.Val1161=
XM_011519021.1:c.3510T= XP_011517323.1:p.Val1170=
XM_011519022.1:c.3507T= XP_011517324.1:p.Val1169=
XM_011519023.1:c.3489T= XP_011517325.1:p.Val1163=
XM_011519024.1:c.3432T= XP_011517326.1:p.Val1144=
XM_011519025.1:c.3408T= XP_011517327.1:p.Val1136=
XM_011519026.1:c.3366T= XP_011517328.1:p.Val1122=
XM_011519029.1:c.1932T= XP_011517331.1:p.Val644=
XM_011519030.1:c.1284T= XP_011517332.1:p.Val428=
XM_011519031.1:c.1071T= XP_011517333.1:p.Val357=
XM_011519032.1:c.1071T= XP_011517334.1:p.Val357=
XM_011519033.1:c.3345T= XP_011517335.1:p.Val1115=
XR_930459.1:n.5297-3537A=
NM_001354263.1:c.3480T= NP_001341192.1:p.Val1160=
XM_005266105.5:c.3492T= XP_005266162.1:p.Val1164=
XM_011519021.3:c.3510T= XP_011517323.1:p.Val1170=
XM_011519022.3:c.3507T= XP_011517324.1:p.Val1169=
XM_011519023.3:c.3489T= XP_011517325.1:p.Val1163=
XM_011519029.3:c.1932T= XP_011517331.1:p.Val644=
XM_011519030.3:c.1284T= XP_011517332.1:p.Val428=
XM_017015134.1:c.3486T= XP_016870623.1:p.Val1162=
XM_017015136.2:c.3402T= XP_016870625.1:p.Val1134=
XM_017015137.1:c.3387T= XP_016870626.1:p.Val1129=
XM_017015138.1:c.3387T= XP_016870627.1:p.Val1129=
XM_024447674.1:c.3330T= XP_024303442.1:p.Val1110=
XM_024447675.1:c.3264T= XP_024303443.1:p.Val1088=
XM_024447676.1:c.2625T= XP_024303444.1:p.Val875=
XM_024447677.1:c.2625T= XP_024303445.1:p.Val875=
XM_024447680.1:c.3243T= XP_024303448.1:p.Val1081=
NM_024757.5:c.3501T= MANE Select NP_079033.4:p.Val1167=
NM_001354263.2:c.3480T= NP_001341192.1:p.Val1160=