Canonical Allele Identifier: CA1884685669
Gene: EHMT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.137813009C= , CM000671.2:g.137813009C= GRCh38
NC_000009.11:g.140707461C= , CM000671.1:g.140707461C= GRCh37
NC_000009.10:g.139827282C= NCBI36
NG_011776.1:g.199018C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000460843.6:c.2871C= MANE Select ENSP00000417980.1:p.Leu957=
ENST00000636027.1:c.2757C= ENSP00000489961.1:p.Leu919=
ENST00000637161.1:c.2778C= ENSP00000490328.1:p.Leu926=
ENST00000637261.1:c.2911C= ENSP00000490815.1:n.2911C=
ENST00000637891.1:c.765C= ENSP00000490907.1:p.Leu255=
ENST00000460843.5:c.2871C= ENSP00000417980.1:p.Leu957=
ENST00000462942.3:c.1728C= ENSP00000436107.1:p.Leu576=
ENST00000486164.5:c.558C=
ENST00000488242.2:n.397C=
NM_024757.4:c.2871C= NP_079033.4:p.Leu957=
XM_005266105.3:c.2862C= XP_005266162.1:p.Leu954=
XM_005266110.1:c.2778C= XP_005266167.1:p.Leu926=
XM_006717288.2:c.2853C= XP_006717351.1:p.Leu951=
XM_011519021.1:c.2880C= XP_011517323.1:p.Leu960=
XM_011519022.1:c.2877C= XP_011517324.1:p.Leu959=
XM_011519023.1:c.2859C= XP_011517325.1:p.Leu953=
XM_011519024.1:c.2802C= XP_011517326.1:p.Leu934=
XM_011519025.1:c.2778C= XP_011517327.1:p.Leu926=
XM_011519026.1:c.2736C= XP_011517328.1:p.Leu912=
XM_011519029.1:c.1302C= XP_011517331.1:p.Leu434=
XM_011519030.1:c.654C= XP_011517332.1:p.Leu218=
XM_011519031.1:c.441C= XP_011517333.1:p.Leu147=
XM_011519032.1:c.441C= XP_011517334.1:p.Leu147=
XM_011519033.1:c.2715C= XP_011517335.1:p.Leu905=
NM_001354263.1:c.2850C= NP_001341192.1:p.Leu950=
XM_005266105.5:c.2862C= XP_005266162.1:p.Leu954=
XM_011519021.3:c.2880C= XP_011517323.1:p.Leu960=
XM_011519022.3:c.2877C= XP_011517324.1:p.Leu959=
XM_011519023.3:c.2859C= XP_011517325.1:p.Leu953=
XM_011519029.3:c.1302C= XP_011517331.1:p.Leu434=
XM_011519030.3:c.654C= XP_011517332.1:p.Leu218=
XM_017015134.1:c.2856C= XP_016870623.1:p.Leu952=
XM_017015136.2:c.2772C= XP_016870625.1:p.Leu924=
XM_017015137.1:c.2757C= XP_016870626.1:p.Leu919=
XM_017015138.1:c.2757C= XP_016870627.1:p.Leu919=
XM_024447674.1:c.2700C= XP_024303442.1:p.Leu900=
XM_024447675.1:c.2634C= XP_024303443.1:p.Leu878=
XM_024447676.1:c.1995C= XP_024303444.1:p.Leu665=
XM_024447677.1:c.1995C= XP_024303445.1:p.Leu665=
XM_024447680.1:c.2613C= XP_024303448.1:p.Leu871=
NM_024757.5:c.2871C= MANE Select NP_079033.4:p.Leu957=
NM_001354263.2:c.2850C= NP_001341192.1:p.Leu950=