Canonical Allele Identifier: CA375791519

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140705974T>G (hg19) ; chr9:g.137811522T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137811522T>G , CM000671.2:g.137811522T>G	GRCh38
NC_000009.11:g.140705974T>G , CM000671.1:g.140705974T>G	GRCh37
NC_000009.10:g.139825795T>G	NCBI36
NG_011776.1:g.197531T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000460843.6:c.2774T>G MANE Select	ENSP00000417980.1:p.Leu925Arg
ENST00000636027.1:c.2660T>G	ENSP00000489961.1:p.Leu887Arg
ENST00000637161.1:c.2681T>G	ENSP00000490328.1:p.Leu894Arg
ENST00000637261.1:c.2814T>G	ENSP00000490815.1:n.2814T>G
ENST00000637891.1:c.668T>G	ENSP00000490907.1:p.Leu223Arg
ENST00000460843.5:c.2774T>G	ENSP00000417980.1:p.Leu925Arg
ENST00000462942.3:c.1631T>G	ENSP00000436107.1:p.Leu544Arg
ENST00000486164.5:c.461T>G
ENST00000488242.2:n.300T>G
NM_024757.4:c.2774T>G	NP_079033.4:p.Leu925Arg
XM_005266105.3:c.2765T>G	XP_005266162.1:p.Leu922Arg
XM_005266110.1:c.2681T>G	XP_005266167.1:p.Leu894Arg
XM_006717288.2:c.2756T>G	XP_006717351.1:p.Leu919Arg
XM_011519021.1:c.2783T>G	XP_011517323.1:p.Leu928Arg
XM_011519022.1:c.2780T>G	XP_011517324.1:p.Leu927Arg
XM_011519023.1:c.2762T>G	XP_011517325.1:p.Leu921Arg
XM_011519024.1:c.2705T>G	XP_011517326.1:p.Leu902Arg
XM_011519025.1:c.2681T>G	XP_011517327.1:p.Leu894Arg
XM_011519026.1:c.2639T>G	XP_011517328.1:p.Leu880Arg
XM_011519029.1:c.1205T>G	XP_011517331.1:p.Leu402Arg
XM_011519030.1:c.557T>G	XP_011517332.1:p.Leu186Arg
XM_011519031.1:c.344T>G	XP_011517333.1:p.Leu115Arg
XM_011519032.1:c.344T>G	XP_011517334.1:p.Leu115Arg
XM_011519033.1:c.2618T>G	XP_011517335.1:p.Leu873Arg
NM_001354263.1:c.2753T>G	NP_001341192.1:p.Leu918Arg
XM_005266105.5:c.2765T>G	XP_005266162.1:p.Leu922Arg
XM_011519021.3:c.2783T>G	XP_011517323.1:p.Leu928Arg
XM_011519022.3:c.2780T>G	XP_011517324.1:p.Leu927Arg
XM_011519023.3:c.2762T>G	XP_011517325.1:p.Leu921Arg
XM_011519029.3:c.1205T>G	XP_011517331.1:p.Leu402Arg
XM_011519030.3:c.557T>G	XP_011517332.1:p.Leu186Arg
XM_017015134.1:c.2759T>G	XP_016870623.1:p.Leu920Arg
XM_017015136.2:c.2675T>G	XP_016870625.1:p.Leu892Arg
XM_017015137.1:c.2660T>G	XP_016870626.1:p.Leu887Arg
XM_017015138.1:c.2660T>G	XP_016870627.1:p.Leu887Arg
XM_024447674.1:c.2603T>G	XP_024303442.1:p.Leu868Arg
XM_024447675.1:c.2537T>G	XP_024303443.1:p.Leu846Arg
XM_024447676.1:c.1898T>G	XP_024303444.1:p.Leu633Arg
XM_024447677.1:c.1898T>G	XP_024303445.1:p.Leu633Arg
XM_024447680.1:c.2516T>G	XP_024303448.1:p.Leu839Arg
NM_024757.5:c.2774T>G MANE Select	NP_079033.4:p.Leu925Arg
NM_001354263.2:c.2753T>G	NP_001341192.1:p.Leu918Arg