Canonical Allele Identifier: CA468161096

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140707596G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137813144G>A , CM000671.2:g.137813144G>A	GRCh38
NC_000009.11:g.140707596G>A , CM000671.1:g.140707596G>A	GRCh37
NC_000009.10:g.139827417G>A	NCBI36
NG_011776.1:g.199153G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.3006G>A MANE Select	ENSP00000417980.1:p.Arg1002=
ENST00000636027.1:c.2892G>A	ENSP00000489961.1:p.Arg964=
ENST00000637161.1:c.2913G>A	ENSP00000490328.1:p.Arg971=
ENST00000637261.1:c.3046G>A	ENSP00000490815.1:n.3046G>A
ENST00000637891.1:c.900G>A	ENSP00000490907.1:p.Arg300=
ENST00000460843.5:c.3006G>A	ENSP00000417980.1:p.Arg1002=
ENST00000462942.3:c.1863G>A	ENSP00000436107.1:p.Arg621=
ENST00000486164.5:c.693G>A
ENST00000488242.2:n.532G>A
NM_024757.4:c.3006G>A	NP_079033.4:p.Arg1002=
XM_005266105.3:c.2997G>A	XP_005266162.1:p.Arg999=
XM_005266110.1:c.2913G>A	XP_005266167.1:p.Arg971=
XM_006717288.2:c.2988G>A	XP_006717351.1:p.Arg996=
XM_011519021.1:c.3015G>A	XP_011517323.1:p.Arg1005=
XM_011519022.1:c.3012G>A	XP_011517324.1:p.Arg1004=
XM_011519023.1:c.2994G>A	XP_011517325.1:p.Arg998=
XM_011519024.1:c.2937G>A	XP_011517326.1:p.Arg979=
XM_011519025.1:c.2913G>A	XP_011517327.1:p.Arg971=
XM_011519026.1:c.2871G>A	XP_011517328.1:p.Arg957=
XM_011519029.1:c.1437G>A	XP_011517331.1:p.Arg479=
XM_011519030.1:c.789G>A	XP_011517332.1:p.Arg263=
XM_011519031.1:c.576G>A	XP_011517333.1:p.Arg192=
XM_011519032.1:c.576G>A	XP_011517334.1:p.Arg192=
XM_011519033.1:c.2850G>A	XP_011517335.1:p.Arg950=
NM_001354263.1:c.2985G>A	NP_001341192.1:p.Arg995=
XM_005266105.5:c.2997G>A	XP_005266162.1:p.Arg999=
XM_011519021.3:c.3015G>A	XP_011517323.1:p.Arg1005=
XM_011519022.3:c.3012G>A	XP_011517324.1:p.Arg1004=
XM_011519023.3:c.2994G>A	XP_011517325.1:p.Arg998=
XM_011519029.3:c.1437G>A	XP_011517331.1:p.Arg479=
XM_011519030.3:c.789G>A	XP_011517332.1:p.Arg263=
XM_017015134.1:c.2991G>A	XP_016870623.1:p.Arg997=
XM_017015136.2:c.2907G>A	XP_016870625.1:p.Arg969=
XM_017015137.1:c.2892G>A	XP_016870626.1:p.Arg964=
XM_017015138.1:c.2892G>A	XP_016870627.1:p.Arg964=
XM_024447674.1:c.2835G>A	XP_024303442.1:p.Arg945=
XM_024447675.1:c.2769G>A	XP_024303443.1:p.Arg923=
XM_024447676.1:c.2130G>A	XP_024303444.1:p.Arg710=
XM_024447677.1:c.2130G>A	XP_024303445.1:p.Arg710=
XM_024447680.1:c.2748G>A	XP_024303448.1:p.Arg916=
NM_024757.5:c.3006G>A MANE Select	NP_079033.4:p.Arg1002=
NM_001354263.2:c.2985G>A	NP_001341192.1:p.Arg995=