Canonical Allele Identifier: CA375793746

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140707625G>C (hg19) ; chr9:g.137813173G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137813173G>C , CM000671.2:g.137813173G>C	GRCh38
NC_000009.11:g.140707625G>C , CM000671.1:g.140707625G>C	GRCh37
NC_000009.10:g.139827446G>C	NCBI36
NG_011776.1:g.199182G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.3035G>C MANE Select	ENSP00000417980.1:p.Arg1012Thr
ENST00000636027.1:c.2921G>C	ENSP00000489961.1:p.Arg974Thr
ENST00000637161.1:c.2942G>C	ENSP00000490328.1:p.Arg981Thr
ENST00000637261.1:c.3075G>C	ENSP00000490815.1:n.3075G>C
ENST00000637891.1:c.929G>C	ENSP00000490907.1:p.Arg310Thr
ENST00000460843.5:c.3035G>C	ENSP00000417980.1:p.Arg1012Thr
ENST00000462942.3:c.1892G>C	ENSP00000436107.1:p.Arg631Thr
ENST00000486164.5:c.722G>C
ENST00000488242.2:n.561G>C
NM_024757.4:c.3035G>C	NP_079033.4:p.Arg1012Thr
XM_005266105.3:c.3026G>C	XP_005266162.1:p.Arg1009Thr
XM_005266110.1:c.2942G>C	XP_005266167.1:p.Arg981Thr
XM_006717288.2:c.3017G>C	XP_006717351.1:p.Arg1006Thr
XM_011519021.1:c.3044G>C	XP_011517323.1:p.Arg1015Thr
XM_011519022.1:c.3041G>C	XP_011517324.1:p.Arg1014Thr
XM_011519023.1:c.3023G>C	XP_011517325.1:p.Arg1008Thr
XM_011519024.1:c.2966G>C	XP_011517326.1:p.Arg989Thr
XM_011519025.1:c.2942G>C	XP_011517327.1:p.Arg981Thr
XM_011519026.1:c.2900G>C	XP_011517328.1:p.Arg967Thr
XM_011519029.1:c.1466G>C	XP_011517331.1:p.Arg489Thr
XM_011519030.1:c.818G>C	XP_011517332.1:p.Arg273Thr
XM_011519031.1:c.605G>C	XP_011517333.1:p.Arg202Thr
XM_011519032.1:c.605G>C	XP_011517334.1:p.Arg202Thr
XM_011519033.1:c.2879G>C	XP_011517335.1:p.Arg960Thr
NM_001354263.1:c.3014G>C	NP_001341192.1:p.Arg1005Thr
XM_005266105.5:c.3026G>C	XP_005266162.1:p.Arg1009Thr
XM_011519021.3:c.3044G>C	XP_011517323.1:p.Arg1015Thr
XM_011519022.3:c.3041G>C	XP_011517324.1:p.Arg1014Thr
XM_011519023.3:c.3023G>C	XP_011517325.1:p.Arg1008Thr
XM_011519029.3:c.1466G>C	XP_011517331.1:p.Arg489Thr
XM_011519030.3:c.818G>C	XP_011517332.1:p.Arg273Thr
XM_017015134.1:c.3020G>C	XP_016870623.1:p.Arg1007Thr
XM_017015136.2:c.2936G>C	XP_016870625.1:p.Arg979Thr
XM_017015137.1:c.2921G>C	XP_016870626.1:p.Arg974Thr
XM_017015138.1:c.2921G>C	XP_016870627.1:p.Arg974Thr
XM_024447674.1:c.2864G>C	XP_024303442.1:p.Arg955Thr
XM_024447675.1:c.2798G>C	XP_024303443.1:p.Arg933Thr
XM_024447676.1:c.2159G>C	XP_024303444.1:p.Arg720Thr
XM_024447677.1:c.2159G>C	XP_024303445.1:p.Arg720Thr
XM_024447680.1:c.2777G>C	XP_024303448.1:p.Arg926Thr
NM_024757.5:c.3035G>C MANE Select	NP_079033.4:p.Arg1012Thr
NM_001354263.2:c.3014G>C	NP_001341192.1:p.Arg1005Thr