Canonical Allele Identifier: CA375793213

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140707472G>C (hg19) ; chr9:g.137813020G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137813020G>C , CM000671.2:g.137813020G>C	GRCh38
NC_000009.11:g.140707472G>C , CM000671.1:g.140707472G>C	GRCh37
NC_000009.10:g.139827293G>C	NCBI36
NG_011776.1:g.199029G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.2882G>C MANE Select	ENSP00000417980.1:p.Arg961Pro
ENST00000636027.1:c.2768G>C	ENSP00000489961.1:p.Arg923Pro
ENST00000637161.1:c.2789G>C	ENSP00000490328.1:p.Arg930Pro
ENST00000637261.1:c.2922G>C	ENSP00000490815.1:n.2922G>C
ENST00000637891.1:c.776G>C	ENSP00000490907.1:p.Arg259Pro
ENST00000460843.5:c.2882G>C	ENSP00000417980.1:p.Arg961Pro
ENST00000462942.3:c.1739G>C	ENSP00000436107.1:p.Arg580Pro
ENST00000486164.5:c.569G>C
ENST00000488242.2:n.408G>C
NM_024757.4:c.2882G>C	NP_079033.4:p.Arg961Pro
XM_005266105.3:c.2873G>C	XP_005266162.1:p.Arg958Pro
XM_005266110.1:c.2789G>C	XP_005266167.1:p.Arg930Pro
XM_006717288.2:c.2864G>C	XP_006717351.1:p.Arg955Pro
XM_011519021.1:c.2891G>C	XP_011517323.1:p.Arg964Pro
XM_011519022.1:c.2888G>C	XP_011517324.1:p.Arg963Pro
XM_011519023.1:c.2870G>C	XP_011517325.1:p.Arg957Pro
XM_011519024.1:c.2813G>C	XP_011517326.1:p.Arg938Pro
XM_011519025.1:c.2789G>C	XP_011517327.1:p.Arg930Pro
XM_011519026.1:c.2747G>C	XP_011517328.1:p.Arg916Pro
XM_011519029.1:c.1313G>C	XP_011517331.1:p.Arg438Pro
XM_011519030.1:c.665G>C	XP_011517332.1:p.Arg222Pro
XM_011519031.1:c.452G>C	XP_011517333.1:p.Arg151Pro
XM_011519032.1:c.452G>C	XP_011517334.1:p.Arg151Pro
XM_011519033.1:c.2726G>C	XP_011517335.1:p.Arg909Pro
NM_001354263.1:c.2861G>C	NP_001341192.1:p.Arg954Pro
XM_005266105.5:c.2873G>C	XP_005266162.1:p.Arg958Pro
XM_011519021.3:c.2891G>C	XP_011517323.1:p.Arg964Pro
XM_011519022.3:c.2888G>C	XP_011517324.1:p.Arg963Pro
XM_011519023.3:c.2870G>C	XP_011517325.1:p.Arg957Pro
XM_011519029.3:c.1313G>C	XP_011517331.1:p.Arg438Pro
XM_011519030.3:c.665G>C	XP_011517332.1:p.Arg222Pro
XM_017015134.1:c.2867G>C	XP_016870623.1:p.Arg956Pro
XM_017015136.2:c.2783G>C	XP_016870625.1:p.Arg928Pro
XM_017015137.1:c.2768G>C	XP_016870626.1:p.Arg923Pro
XM_017015138.1:c.2768G>C	XP_016870627.1:p.Arg923Pro
XM_024447674.1:c.2711G>C	XP_024303442.1:p.Arg904Pro
XM_024447675.1:c.2645G>C	XP_024303443.1:p.Arg882Pro
XM_024447676.1:c.2006G>C	XP_024303444.1:p.Arg669Pro
XM_024447677.1:c.2006G>C	XP_024303445.1:p.Arg669Pro
XM_024447680.1:c.2624G>C	XP_024303448.1:p.Arg875Pro
NM_024757.5:c.2882G>C MANE Select	NP_079033.4:p.Arg961Pro
NM_001354263.2:c.2861G>C	NP_001341192.1:p.Arg954Pro