Canonical Allele Identifier: CA375794551

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140707963G>C (hg19) ; chr9:g.137813511G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137813511G>C , CM000671.2:g.137813511G>C	GRCh38
NC_000009.11:g.140707963G>C , CM000671.1:g.140707963G>C	GRCh37
NC_000009.10:g.139827784G>C	NCBI36
NG_011776.1:g.199520G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.3161G>C MANE Select	ENSP00000417980.1:p.Arg1054Thr
ENST00000637161.1:c.3068G>C	ENSP00000490328.1:p.Arg1023Thr
ENST00000637261.1:c.3201G>C	ENSP00000490815.1:n.3201G>C
ENST00000637891.1:c.1055G>C	ENSP00000490907.1:p.Arg352Thr
ENST00000460843.5:c.3161G>C	ENSP00000417980.1:p.Arg1054Thr
ENST00000462942.3:c.2018G>C	ENSP00000436107.1:p.Arg673Thr
ENST00000483653.1:n.21G>C
ENST00000488242.2:n.687G>C
NM_024757.4:c.3161G>C	NP_079033.4:p.Arg1054Thr
XM_005266105.3:c.3152G>C	XP_005266162.1:p.Arg1051Thr
XM_005266110.1:c.3068G>C	XP_005266167.1:p.Arg1023Thr
XM_006717288.2:c.3143G>C	XP_006717351.1:p.Arg1048Thr
XM_011519021.1:c.3170G>C	XP_011517323.1:p.Arg1057Thr
XM_011519022.1:c.3167G>C	XP_011517324.1:p.Arg1056Thr
XM_011519023.1:c.3149G>C	XP_011517325.1:p.Arg1050Thr
XM_011519024.1:c.3092G>C	XP_011517326.1:p.Arg1031Thr
XM_011519025.1:c.3068G>C	XP_011517327.1:p.Arg1023Thr
XM_011519026.1:c.3026G>C	XP_011517328.1:p.Arg1009Thr
XM_011519029.1:c.1592G>C	XP_011517331.1:p.Arg531Thr
XM_011519030.1:c.944G>C	XP_011517332.1:p.Arg315Thr
XM_011519031.1:c.731G>C	XP_011517333.1:p.Arg244Thr
XM_011519032.1:c.731G>C	XP_011517334.1:p.Arg244Thr
XM_011519033.1:c.3005G>C	XP_011517335.1:p.Arg1002Thr
NM_001354263.1:c.3140G>C	NP_001341192.1:p.Arg1047Thr
XM_005266105.5:c.3152G>C	XP_005266162.1:p.Arg1051Thr
XM_011519021.3:c.3170G>C	XP_011517323.1:p.Arg1057Thr
XM_011519022.3:c.3167G>C	XP_011517324.1:p.Arg1056Thr
XM_011519023.3:c.3149G>C	XP_011517325.1:p.Arg1050Thr
XM_011519029.3:c.1592G>C	XP_011517331.1:p.Arg531Thr
XM_011519030.3:c.944G>C	XP_011517332.1:p.Arg315Thr
XM_017015134.1:c.3146G>C	XP_016870623.1:p.Arg1049Thr
XM_017015136.2:c.3062G>C	XP_016870625.1:p.Arg1021Thr
XM_017015137.1:c.3047G>C	XP_016870626.1:p.Arg1016Thr
XM_017015138.1:c.3047G>C	XP_016870627.1:p.Arg1016Thr
XM_024447674.1:c.2990G>C	XP_024303442.1:p.Arg997Thr
XM_024447675.1:c.2924G>C	XP_024303443.1:p.Arg975Thr
XM_024447676.1:c.2285G>C	XP_024303444.1:p.Arg762Thr
XM_024447677.1:c.2285G>C	XP_024303445.1:p.Arg762Thr
XM_024447680.1:c.2903G>C	XP_024303448.1:p.Arg968Thr
NM_024757.5:c.3161G>C MANE Select	NP_079033.4:p.Arg1054Thr
NM_001354263.2:c.3140G>C	NP_001341192.1:p.Arg1047Thr