Canonical Allele Identifier: CA375793828

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140707849G>C (hg19) ; chr9:g.137813397G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137813397G>C , CM000671.2:g.137813397G>C	GRCh38
NC_000009.11:g.140707849G>C , CM000671.1:g.140707849G>C	GRCh37
NC_000009.10:g.139827670G>C	NCBI36
NG_011776.1:g.199406G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.3047G>C MANE Select	ENSP00000417980.1:p.Arg1016Pro
ENST00000636027.1:c.2933G>C	ENSP00000489961.1:p.Arg978Pro
ENST00000637161.1:c.2954G>C	ENSP00000490328.1:p.Arg985Pro
ENST00000637261.1:c.3087G>C	ENSP00000490815.1:n.3087G>C
ENST00000637891.1:c.941G>C	ENSP00000490907.1:p.Arg314Pro
ENST00000460843.5:c.3047G>C	ENSP00000417980.1:p.Arg1016Pro
ENST00000462942.3:c.1904G>C	ENSP00000436107.1:p.Arg635Pro
ENST00000486164.5:c.734G>C
ENST00000488242.2:n.573G>C
NM_024757.4:c.3047G>C	NP_079033.4:p.Arg1016Pro
XM_005266105.3:c.3038G>C	XP_005266162.1:p.Arg1013Pro
XM_005266110.1:c.2954G>C	XP_005266167.1:p.Arg985Pro
XM_006717288.2:c.3029G>C	XP_006717351.1:p.Arg1010Pro
XM_011519021.1:c.3056G>C	XP_011517323.1:p.Arg1019Pro
XM_011519022.1:c.3053G>C	XP_011517324.1:p.Arg1018Pro
XM_011519023.1:c.3035G>C	XP_011517325.1:p.Arg1012Pro
XM_011519024.1:c.2978G>C	XP_011517326.1:p.Arg993Pro
XM_011519025.1:c.2954G>C	XP_011517327.1:p.Arg985Pro
XM_011519026.1:c.2912G>C	XP_011517328.1:p.Arg971Pro
XM_011519029.1:c.1478G>C	XP_011517331.1:p.Arg493Pro
XM_011519030.1:c.830G>C	XP_011517332.1:p.Arg277Pro
XM_011519031.1:c.617G>C	XP_011517333.1:p.Arg206Pro
XM_011519032.1:c.617G>C	XP_011517334.1:p.Arg206Pro
XM_011519033.1:c.2891G>C	XP_011517335.1:p.Arg964Pro
NM_001354263.1:c.3026G>C	NP_001341192.1:p.Arg1009Pro
XM_005266105.5:c.3038G>C	XP_005266162.1:p.Arg1013Pro
XM_011519021.3:c.3056G>C	XP_011517323.1:p.Arg1019Pro
XM_011519022.3:c.3053G>C	XP_011517324.1:p.Arg1018Pro
XM_011519023.3:c.3035G>C	XP_011517325.1:p.Arg1012Pro
XM_011519029.3:c.1478G>C	XP_011517331.1:p.Arg493Pro
XM_011519030.3:c.830G>C	XP_011517332.1:p.Arg277Pro
XM_017015134.1:c.3032G>C	XP_016870623.1:p.Arg1011Pro
XM_017015136.2:c.2948G>C	XP_016870625.1:p.Arg983Pro
XM_017015137.1:c.2933G>C	XP_016870626.1:p.Arg978Pro
XM_017015138.1:c.2933G>C	XP_016870627.1:p.Arg978Pro
XM_024447674.1:c.2876G>C	XP_024303442.1:p.Arg959Pro
XM_024447675.1:c.2810G>C	XP_024303443.1:p.Arg937Pro
XM_024447676.1:c.2171G>C	XP_024303444.1:p.Arg724Pro
XM_024447677.1:c.2171G>C	XP_024303445.1:p.Arg724Pro
XM_024447680.1:c.2789G>C	XP_024303448.1:p.Arg930Pro
NM_024757.5:c.3047G>C MANE Select	NP_079033.4:p.Arg1016Pro
NM_001354263.2:c.3026G>C	NP_001341192.1:p.Arg1009Pro