Canonical Allele Identifier: CA1884679284
Gene: EHMT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.137800955A= , CM000671.2:g.137800955A= GRCh38
NC_000009.11:g.140695407A= , CM000671.1:g.140695407A= GRCh37
NC_000009.10:g.139815228A= NCBI36
NG_011776.1:g.186964A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000460843.6:c.2683A= MANE Select ENSP00000417980.1:p.Lys895=
ENST00000636027.1:c.2569A= ENSP00000489961.1:p.Lys857=
ENST00000637161.1:c.2590A= ENSP00000490328.1:p.Lys864=
ENST00000637261.1:c.2723A= ENSP00000490815.1:n.2723A=
ENST00000637891.1:c.577A= ENSP00000490907.1:p.Lys193=
ENST00000637949.1:c.361A= ENSP00000489786.1:p.Lys121=
ENST00000460843.5:c.2683A= ENSP00000417980.1:p.Lys895=
ENST00000462942.3:c.1540A= ENSP00000436107.1:p.Lys514=
ENST00000482340.5:c.253A= ENSP00000486748.1:p.Lys85=
ENST00000486164.5:c.261A=
ENST00000488242.2:n.209A=
ENST00000493484.5:c.253A= ENSP00000486503.1:p.Lys85=
NM_024757.4:c.2683A= NP_079033.4:p.Lys895=
XM_005266105.3:c.2674A= XP_005266162.1:p.Lys892=
XM_005266110.1:c.2590A= XP_005266167.1:p.Lys864=
XM_006717288.2:c.2665A= XP_006717351.1:p.Lys889=
XM_011519021.1:c.2692A= XP_011517323.1:p.Lys898=
XM_011519022.1:c.2689A= XP_011517324.1:p.Lys897=
XM_011519023.1:c.2671A= XP_011517325.1:p.Lys891=
XM_011519024.1:c.2614A= XP_011517326.1:p.Lys872=
XM_011519025.1:c.2590A= XP_011517327.1:p.Lys864=
XM_011519026.1:c.2548A= XP_011517328.1:p.Lys850=
XM_011519027.1:c.2692A= XP_011517329.1:p.Lys898=
XM_011519029.1:c.1114A= XP_011517331.1:p.Lys372=
XM_011519030.1:c.466A= XP_011517332.1:p.Lys156=
XM_011519031.1:c.253A= XP_011517333.1:p.Lys85=
XM_011519032.1:c.253A= XP_011517334.1:p.Lys85=
XM_011519033.1:c.2527A= XP_011517335.1:p.Lys843=
NM_001354263.1:c.2662A= NP_001341192.1:p.Lys888=
XM_005266105.5:c.2674A= XP_005266162.1:p.Lys892=
XM_011519021.3:c.2692A= XP_011517323.1:p.Lys898=
XM_011519022.3:c.2689A= XP_011517324.1:p.Lys897=
XM_011519023.3:c.2671A= XP_011517325.1:p.Lys891=
XM_011519029.3:c.1114A= XP_011517331.1:p.Lys372=
XM_011519030.3:c.466A= XP_011517332.1:p.Lys156=
XM_017015134.1:c.2668A= XP_016870623.1:p.Lys890=
XM_017015136.2:c.2584A= XP_016870625.1:p.Lys862=
XM_017015137.1:c.2569A= XP_016870626.1:p.Lys857=
XM_017015138.1:c.2569A= XP_016870627.1:p.Lys857=
XM_024447674.1:c.2512A= XP_024303442.1:p.Lys838=
XM_024447675.1:c.2446A= XP_024303443.1:p.Lys816=
XM_024447676.1:c.1807A= XP_024303444.1:p.Lys603=
XM_024447677.1:c.1807A= XP_024303445.1:p.Lys603=
XM_024447678.1:c.2590A= XP_024303446.1:p.Lys864=
XM_024447680.1:c.2425A= XP_024303448.1:p.Lys809=
NM_024757.5:c.2683A= MANE Select NP_079033.4:p.Lys895=
NM_001354263.2:c.2662A= NP_001341192.1:p.Lys888=