Canonical Allele Identifier: CA1884685695
Gene: EHMT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.137813086C= , CM000671.2:g.137813086C= GRCh38
NC_000009.11:g.140707538C= , CM000671.1:g.140707538C= GRCh37
NC_000009.10:g.139827359C= NCBI36
NG_011776.1:g.199095C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000460843.6:c.2948C= MANE Select ENSP00000417980.1:p.Ser983=
ENST00000636027.1:c.2834C= ENSP00000489961.1:p.Ser945=
ENST00000637161.1:c.2855C= ENSP00000490328.1:p.Ser952=
ENST00000637261.1:c.2988C= ENSP00000490815.1:n.2988C=
ENST00000637891.1:c.842C= ENSP00000490907.1:p.Ser281=
ENST00000460843.5:c.2948C= ENSP00000417980.1:p.Ser983=
ENST00000462942.3:c.1805C= ENSP00000436107.1:p.Ser602=
ENST00000486164.5:c.635C=
ENST00000488242.2:n.474C=
NM_024757.4:c.2948C= NP_079033.4:p.Ser983=
XM_005266105.3:c.2939C= XP_005266162.1:p.Ser980=
XM_005266110.1:c.2855C= XP_005266167.1:p.Ser952=
XM_006717288.2:c.2930C= XP_006717351.1:p.Ser977=
XM_011519021.1:c.2957C= XP_011517323.1:p.Ser986=
XM_011519022.1:c.2954C= XP_011517324.1:p.Ser985=
XM_011519023.1:c.2936C= XP_011517325.1:p.Ser979=
XM_011519024.1:c.2879C= XP_011517326.1:p.Ser960=
XM_011519025.1:c.2855C= XP_011517327.1:p.Ser952=
XM_011519026.1:c.2813C= XP_011517328.1:p.Ser938=
XM_011519029.1:c.1379C= XP_011517331.1:p.Ser460=
XM_011519030.1:c.731C= XP_011517332.1:p.Ser244=
XM_011519031.1:c.518C= XP_011517333.1:p.Ser173=
XM_011519032.1:c.518C= XP_011517334.1:p.Ser173=
XM_011519033.1:c.2792C= XP_011517335.1:p.Ser931=
NM_001354263.1:c.2927C= NP_001341192.1:p.Ser976=
XM_005266105.5:c.2939C= XP_005266162.1:p.Ser980=
XM_011519021.3:c.2957C= XP_011517323.1:p.Ser986=
XM_011519022.3:c.2954C= XP_011517324.1:p.Ser985=
XM_011519023.3:c.2936C= XP_011517325.1:p.Ser979=
XM_011519029.3:c.1379C= XP_011517331.1:p.Ser460=
XM_011519030.3:c.731C= XP_011517332.1:p.Ser244=
XM_017015134.1:c.2933C= XP_016870623.1:p.Ser978=
XM_017015136.2:c.2849C= XP_016870625.1:p.Ser950=
XM_017015137.1:c.2834C= XP_016870626.1:p.Ser945=
XM_017015138.1:c.2834C= XP_016870627.1:p.Ser945=
XM_024447674.1:c.2777C= XP_024303442.1:p.Ser926=
XM_024447675.1:c.2711C= XP_024303443.1:p.Ser904=
XM_024447676.1:c.2072C= XP_024303444.1:p.Ser691=
XM_024447677.1:c.2072C= XP_024303445.1:p.Ser691=
XM_024447680.1:c.2690C= XP_024303448.1:p.Ser897=
NM_024757.5:c.2948C= MANE Select NP_079033.4:p.Ser983=
NM_001354263.2:c.2927C= NP_001341192.1:p.Ser976=