Canonical Allele Identifier: CA1884688379
Gene: EHMT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.137818135T= , CM000671.2:g.137818135T= GRCh38
NC_000009.11:g.140712587T= , CM000671.1:g.140712587T= GRCh37
NC_000009.10:g.139832408T= NCBI36
NG_011776.1:g.204144T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000460843.6:c.3537T= MANE Select ENSP00000417980.1:p.Asn1179=
ENST00000636472.1:n.99T=
ENST00000636526.1:n.23T=
ENST00000637161.1:c.3444T= ENSP00000490328.1:p.Asn1148=
ENST00000637261.1:c.4111T= ENSP00000490815.1:n.4111T=
ENST00000637748.1:n.518T=
ENST00000637891.1:c.1611T= ENSP00000490907.1:n.1611T=
ENST00000460843.5:c.3537T= ENSP00000417980.1:p.Asn1179=
ENST00000462942.3:c.2394T= ENSP00000436107.1:p.Asn798=
ENST00000475564.5:n.1261T=
ENST00000494249.5:n.890T=
NM_024757.4:c.3537T= NP_079033.4:p.Asn1179=
XM_005266105.3:c.3528T= XP_005266162.1:p.Asn1176=
XM_005266110.1:c.3444T= XP_005266167.1:p.Asn1148=
XM_006717288.2:c.3519T= XP_006717351.1:p.Asn1173=
XM_011519021.1:c.3546T= XP_011517323.1:p.Asn1182=
XM_011519022.1:c.3543T= XP_011517324.1:p.Asn1181=
XM_011519023.1:c.3525T= XP_011517325.1:p.Asn1175=
XM_011519024.1:c.3468T= XP_011517326.1:p.Asn1156=
XM_011519025.1:c.3444T= XP_011517327.1:p.Asn1148=
XM_011519026.1:c.3402T= XP_011517328.1:p.Asn1134=
XM_011519029.1:c.1968T= XP_011517331.1:p.Asn656=
XM_011519030.1:c.1320T= XP_011517332.1:p.Asn440=
XM_011519031.1:c.1107T= XP_011517333.1:p.Asn369=
XM_011519032.1:c.1107T= XP_011517334.1:p.Asn369=
XM_011519033.1:c.3381T= XP_011517335.1:p.Asn1127=
XR_930459.1:n.5297-3573A=
NM_001354263.1:c.3516T= NP_001341192.1:p.Asn1172=
XM_005266105.5:c.3528T= XP_005266162.1:p.Asn1176=
XM_011519021.3:c.3546T= XP_011517323.1:p.Asn1182=
XM_011519022.3:c.3543T= XP_011517324.1:p.Asn1181=
XM_011519023.3:c.3525T= XP_011517325.1:p.Asn1175=
XM_011519029.3:c.1968T= XP_011517331.1:p.Asn656=
XM_011519030.3:c.1320T= XP_011517332.1:p.Asn440=
XM_017015134.1:c.3522T= XP_016870623.1:p.Asn1174=
XM_017015136.2:c.3438T= XP_016870625.1:p.Asn1146=
XM_017015137.1:c.3423T= XP_016870626.1:p.Asn1141=
XM_017015138.1:c.3423T= XP_016870627.1:p.Asn1141=
XM_024447674.1:c.3366T= XP_024303442.1:p.Asn1122=
XM_024447675.1:c.3300T= XP_024303443.1:p.Asn1100=
XM_024447676.1:c.2661T= XP_024303444.1:p.Asn887=
XM_024447677.1:c.2661T= XP_024303445.1:p.Asn887=
XM_024447680.1:c.3279T= XP_024303448.1:p.Asn1093=
NM_024757.5:c.3537T= MANE Select NP_079033.4:p.Asn1179=
NM_001354263.2:c.3516T= NP_001341192.1:p.Asn1172=