Canonical Allele Identifier: CA468161396

Gene: EHMT1

Linked Data

• dbSNP Id: rs886063738
• gnomAD v3: 9-137813386-G-A
• gnomAD v4: 9-137813386-G-A
• MyVariant Identifiers: chr9:g.140707838G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137813386G>A , CM000671.2:g.137813386G>A	GRCh38
NC_000009.11:g.140707838G>A , CM000671.1:g.140707838G>A	GRCh37
NC_000009.10:g.139827659G>A	NCBI36
NG_011776.1:g.199395G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.3036G>A MANE Select	ENSP00000417980.1:p.Arg1012=
ENST00000636027.1:c.2922G>A	ENSP00000489961.1:p.Arg974=
ENST00000637161.1:c.2943G>A	ENSP00000490328.1:p.Arg981=
ENST00000637261.1:c.3076G>A	ENSP00000490815.1:n.3076G>A
ENST00000637891.1:c.930G>A	ENSP00000490907.1:p.Arg310=
ENST00000460843.5:c.3036G>A	ENSP00000417980.1:p.Arg1012=
ENST00000462942.3:c.1893G>A	ENSP00000436107.1:p.Arg631=
ENST00000486164.5:c.723G>A
ENST00000488242.2:n.562G>A
NM_024757.4:c.3036G>A	NP_079033.4:p.Arg1012=
XM_005266105.3:c.3027G>A	XP_005266162.1:p.Arg1009=
XM_005266110.1:c.2943G>A	XP_005266167.1:p.Arg981=
XM_006717288.2:c.3018G>A	XP_006717351.1:p.Arg1006=
XM_011519021.1:c.3045G>A	XP_011517323.1:p.Arg1015=
XM_011519022.1:c.3042G>A	XP_011517324.1:p.Arg1014=
XM_011519023.1:c.3024G>A	XP_011517325.1:p.Arg1008=
XM_011519024.1:c.2967G>A	XP_011517326.1:p.Arg989=
XM_011519025.1:c.2943G>A	XP_011517327.1:p.Arg981=
XM_011519026.1:c.2901G>A	XP_011517328.1:p.Arg967=
XM_011519029.1:c.1467G>A	XP_011517331.1:p.Arg489=
XM_011519030.1:c.819G>A	XP_011517332.1:p.Arg273=
XM_011519031.1:c.606G>A	XP_011517333.1:p.Arg202=
XM_011519032.1:c.606G>A	XP_011517334.1:p.Arg202=
XM_011519033.1:c.2880G>A	XP_011517335.1:p.Arg960=
NM_001354263.1:c.3015G>A	NP_001341192.1:p.Arg1005=
XM_005266105.5:c.3027G>A	XP_005266162.1:p.Arg1009=
XM_011519021.3:c.3045G>A	XP_011517323.1:p.Arg1015=
XM_011519022.3:c.3042G>A	XP_011517324.1:p.Arg1014=
XM_011519023.3:c.3024G>A	XP_011517325.1:p.Arg1008=
XM_011519029.3:c.1467G>A	XP_011517331.1:p.Arg489=
XM_011519030.3:c.819G>A	XP_011517332.1:p.Arg273=
XM_017015134.1:c.3021G>A	XP_016870623.1:p.Arg1007=
XM_017015136.2:c.2937G>A	XP_016870625.1:p.Arg979=
XM_017015137.1:c.2922G>A	XP_016870626.1:p.Arg974=
XM_017015138.1:c.2922G>A	XP_016870627.1:p.Arg974=
XM_024447674.1:c.2865G>A	XP_024303442.1:p.Arg955=
XM_024447675.1:c.2799G>A	XP_024303443.1:p.Arg933=
XM_024447676.1:c.2160G>A	XP_024303444.1:p.Arg720=
XM_024447677.1:c.2160G>A	XP_024303445.1:p.Arg720=
XM_024447680.1:c.2778G>A	XP_024303448.1:p.Arg926=
NM_024757.5:c.3036G>A MANE Select	NP_079033.4:p.Arg1012=
NM_001354263.2:c.3015G>A	NP_001341192.1:p.Arg1005=