Canonical Allele Identifier: CA1884685692
Gene: EHMT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.137813082A= , CM000671.2:g.137813082A= GRCh38
NC_000009.11:g.140707534A= , CM000671.1:g.140707534A= GRCh37
NC_000009.10:g.139827355A= NCBI36
NG_011776.1:g.199091A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000460843.6:c.2944A= MANE Select ENSP00000417980.1:p.Asn982=
ENST00000636027.1:c.2830A= ENSP00000489961.1:p.Asn944=
ENST00000637161.1:c.2851A= ENSP00000490328.1:p.Asn951=
ENST00000637261.1:c.2984A= ENSP00000490815.1:n.2984A=
ENST00000637891.1:c.838A= ENSP00000490907.1:p.Asn280=
ENST00000460843.5:c.2944A= ENSP00000417980.1:p.Asn982=
ENST00000462942.3:c.1801A= ENSP00000436107.1:p.Asn601=
ENST00000486164.5:c.631A=
ENST00000488242.2:n.470A=
NM_024757.4:c.2944A= NP_079033.4:p.Asn982=
XM_005266105.3:c.2935A= XP_005266162.1:p.Asn979=
XM_005266110.1:c.2851A= XP_005266167.1:p.Asn951=
XM_006717288.2:c.2926A= XP_006717351.1:p.Asn976=
XM_011519021.1:c.2953A= XP_011517323.1:p.Asn985=
XM_011519022.1:c.2950A= XP_011517324.1:p.Asn984=
XM_011519023.1:c.2932A= XP_011517325.1:p.Asn978=
XM_011519024.1:c.2875A= XP_011517326.1:p.Asn959=
XM_011519025.1:c.2851A= XP_011517327.1:p.Asn951=
XM_011519026.1:c.2809A= XP_011517328.1:p.Asn937=
XM_011519029.1:c.1375A= XP_011517331.1:p.Asn459=
XM_011519030.1:c.727A= XP_011517332.1:p.Asn243=
XM_011519031.1:c.514A= XP_011517333.1:p.Asn172=
XM_011519032.1:c.514A= XP_011517334.1:p.Asn172=
XM_011519033.1:c.2788A= XP_011517335.1:p.Asn930=
NM_001354263.1:c.2923A= NP_001341192.1:p.Asn975=
XM_005266105.5:c.2935A= XP_005266162.1:p.Asn979=
XM_011519021.3:c.2953A= XP_011517323.1:p.Asn985=
XM_011519022.3:c.2950A= XP_011517324.1:p.Asn984=
XM_011519023.3:c.2932A= XP_011517325.1:p.Asn978=
XM_011519029.3:c.1375A= XP_011517331.1:p.Asn459=
XM_011519030.3:c.727A= XP_011517332.1:p.Asn243=
XM_017015134.1:c.2929A= XP_016870623.1:p.Asn977=
XM_017015136.2:c.2845A= XP_016870625.1:p.Asn949=
XM_017015137.1:c.2830A= XP_016870626.1:p.Asn944=
XM_017015138.1:c.2830A= XP_016870627.1:p.Asn944=
XM_024447674.1:c.2773A= XP_024303442.1:p.Asn925=
XM_024447675.1:c.2707A= XP_024303443.1:p.Asn903=
XM_024447676.1:c.2068A= XP_024303444.1:p.Asn690=
XM_024447677.1:c.2068A= XP_024303445.1:p.Asn690=
XM_024447680.1:c.2686A= XP_024303448.1:p.Asn896=
NM_024757.5:c.2944A= MANE Select NP_079033.4:p.Asn982=
NM_001354263.2:c.2923A= NP_001341192.1:p.Asn975=