Canonical Allele Identifier: CA468161028

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140707476T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137813024T>C , CM000671.2:g.137813024T>C	GRCh38
NC_000009.11:g.140707476T>C , CM000671.1:g.140707476T>C	GRCh37
NC_000009.10:g.139827297T>C	NCBI36
NG_011776.1:g.199033T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.2886T>C MANE Select	ENSP00000417980.1:p.Asp962=
ENST00000636027.1:c.2772T>C	ENSP00000489961.1:p.Asp924=
ENST00000637161.1:c.2793T>C	ENSP00000490328.1:p.Asp931=
ENST00000637261.1:c.2926T>C	ENSP00000490815.1:n.2926T>C
ENST00000637891.1:c.780T>C	ENSP00000490907.1:p.Asp260=
ENST00000460843.5:c.2886T>C	ENSP00000417980.1:p.Asp962=
ENST00000462942.3:c.1743T>C	ENSP00000436107.1:p.Asp581=
ENST00000486164.5:c.573T>C
ENST00000488242.2:n.412T>C
NM_024757.4:c.2886T>C	NP_079033.4:p.Asp962=
XM_005266105.3:c.2877T>C	XP_005266162.1:p.Asp959=
XM_005266110.1:c.2793T>C	XP_005266167.1:p.Asp931=
XM_006717288.2:c.2868T>C	XP_006717351.1:p.Asp956=
XM_011519021.1:c.2895T>C	XP_011517323.1:p.Asp965=
XM_011519022.1:c.2892T>C	XP_011517324.1:p.Asp964=
XM_011519023.1:c.2874T>C	XP_011517325.1:p.Asp958=
XM_011519024.1:c.2817T>C	XP_011517326.1:p.Asp939=
XM_011519025.1:c.2793T>C	XP_011517327.1:p.Asp931=
XM_011519026.1:c.2751T>C	XP_011517328.1:p.Asp917=
XM_011519029.1:c.1317T>C	XP_011517331.1:p.Asp439=
XM_011519030.1:c.669T>C	XP_011517332.1:p.Asp223=
XM_011519031.1:c.456T>C	XP_011517333.1:p.Asp152=
XM_011519032.1:c.456T>C	XP_011517334.1:p.Asp152=
XM_011519033.1:c.2730T>C	XP_011517335.1:p.Asp910=
NM_001354263.1:c.2865T>C	NP_001341192.1:p.Asp955=
XM_005266105.5:c.2877T>C	XP_005266162.1:p.Asp959=
XM_011519021.3:c.2895T>C	XP_011517323.1:p.Asp965=
XM_011519022.3:c.2892T>C	XP_011517324.1:p.Asp964=
XM_011519023.3:c.2874T>C	XP_011517325.1:p.Asp958=
XM_011519029.3:c.1317T>C	XP_011517331.1:p.Asp439=
XM_011519030.3:c.669T>C	XP_011517332.1:p.Asp223=
XM_017015134.1:c.2871T>C	XP_016870623.1:p.Asp957=
XM_017015136.2:c.2787T>C	XP_016870625.1:p.Asp929=
XM_017015137.1:c.2772T>C	XP_016870626.1:p.Asp924=
XM_017015138.1:c.2772T>C	XP_016870627.1:p.Asp924=
XM_024447674.1:c.2715T>C	XP_024303442.1:p.Asp905=
XM_024447675.1:c.2649T>C	XP_024303443.1:p.Asp883=
XM_024447676.1:c.2010T>C	XP_024303444.1:p.Asp670=
XM_024447677.1:c.2010T>C	XP_024303445.1:p.Asp670=
XM_024447680.1:c.2628T>C	XP_024303448.1:p.Asp876=
NM_024757.5:c.2886T>C MANE Select	NP_079033.4:p.Asp962=
NM_001354263.2:c.2865T>C	NP_001341192.1:p.Asp955=