Canonical Allele Identifier: CA1884685672
Gene: EHMT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.137813017C= , CM000671.2:g.137813017C= GRCh38
NC_000009.11:g.140707469C= , CM000671.1:g.140707469C= GRCh37
NC_000009.10:g.139827290C= NCBI36
NG_011776.1:g.199026C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000460843.6:c.2879C= MANE Select ENSP00000417980.1:p.Ser960=
ENST00000636027.1:c.2765C= ENSP00000489961.1:p.Ser922=
ENST00000637161.1:c.2786C= ENSP00000490328.1:p.Ser929=
ENST00000637261.1:c.2919C= ENSP00000490815.1:n.2919C=
ENST00000637891.1:c.773C= ENSP00000490907.1:p.Ser258=
ENST00000460843.5:c.2879C= ENSP00000417980.1:p.Ser960=
ENST00000462942.3:c.1736C= ENSP00000436107.1:p.Ser579=
ENST00000486164.5:c.566C=
ENST00000488242.2:n.405C=
NM_024757.4:c.2879C= NP_079033.4:p.Ser960=
XM_005266105.3:c.2870C= XP_005266162.1:p.Ser957=
XM_005266110.1:c.2786C= XP_005266167.1:p.Ser929=
XM_006717288.2:c.2861C= XP_006717351.1:p.Ser954=
XM_011519021.1:c.2888C= XP_011517323.1:p.Ser963=
XM_011519022.1:c.2885C= XP_011517324.1:p.Ser962=
XM_011519023.1:c.2867C= XP_011517325.1:p.Ser956=
XM_011519024.1:c.2810C= XP_011517326.1:p.Ser937=
XM_011519025.1:c.2786C= XP_011517327.1:p.Ser929=
XM_011519026.1:c.2744C= XP_011517328.1:p.Ser915=
XM_011519029.1:c.1310C= XP_011517331.1:p.Ser437=
XM_011519030.1:c.662C= XP_011517332.1:p.Ser221=
XM_011519031.1:c.449C= XP_011517333.1:p.Ser150=
XM_011519032.1:c.449C= XP_011517334.1:p.Ser150=
XM_011519033.1:c.2723C= XP_011517335.1:p.Ser908=
NM_001354263.1:c.2858C= NP_001341192.1:p.Ser953=
XM_005266105.5:c.2870C= XP_005266162.1:p.Ser957=
XM_011519021.3:c.2888C= XP_011517323.1:p.Ser963=
XM_011519022.3:c.2885C= XP_011517324.1:p.Ser962=
XM_011519023.3:c.2867C= XP_011517325.1:p.Ser956=
XM_011519029.3:c.1310C= XP_011517331.1:p.Ser437=
XM_011519030.3:c.662C= XP_011517332.1:p.Ser221=
XM_017015134.1:c.2864C= XP_016870623.1:p.Ser955=
XM_017015136.2:c.2780C= XP_016870625.1:p.Ser927=
XM_017015137.1:c.2765C= XP_016870626.1:p.Ser922=
XM_017015138.1:c.2765C= XP_016870627.1:p.Ser922=
XM_024447674.1:c.2708C= XP_024303442.1:p.Ser903=
XM_024447675.1:c.2642C= XP_024303443.1:p.Ser881=
XM_024447676.1:c.2003C= XP_024303444.1:p.Ser668=
XM_024447677.1:c.2003C= XP_024303445.1:p.Ser668=
XM_024447680.1:c.2621C= XP_024303448.1:p.Ser874=
NM_024757.5:c.2879C= MANE Select NP_079033.4:p.Ser960=
NM_001354263.2:c.2858C= NP_001341192.1:p.Ser953=