Canonical Allele Identifier: CA375793604

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140707568A>G (hg19) ; chr9:g.137813116A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137813116A>G , CM000671.2:g.137813116A>G	GRCh38
NC_000009.11:g.140707568A>G , CM000671.1:g.140707568A>G	GRCh37
NC_000009.10:g.139827389A>G	NCBI36
NG_011776.1:g.199125A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.2978A>G MANE Select	ENSP00000417980.1:p.Lys993Arg
ENST00000636027.1:c.2864A>G	ENSP00000489961.1:p.Lys955Arg
ENST00000637161.1:c.2885A>G	ENSP00000490328.1:p.Lys962Arg
ENST00000637261.1:c.3018A>G	ENSP00000490815.1:n.3018A>G
ENST00000637891.1:c.872A>G	ENSP00000490907.1:p.Lys291Arg
ENST00000460843.5:c.2978A>G	ENSP00000417980.1:p.Lys993Arg
ENST00000462942.3:c.1835A>G	ENSP00000436107.1:p.Lys612Arg
ENST00000486164.5:c.665A>G
ENST00000488242.2:n.504A>G
NM_024757.4:c.2978A>G	NP_079033.4:p.Lys993Arg
XM_005266105.3:c.2969A>G	XP_005266162.1:p.Lys990Arg
XM_005266110.1:c.2885A>G	XP_005266167.1:p.Lys962Arg
XM_006717288.2:c.2960A>G	XP_006717351.1:p.Lys987Arg
XM_011519021.1:c.2987A>G	XP_011517323.1:p.Lys996Arg
XM_011519022.1:c.2984A>G	XP_011517324.1:p.Lys995Arg
XM_011519023.1:c.2966A>G	XP_011517325.1:p.Lys989Arg
XM_011519024.1:c.2909A>G	XP_011517326.1:p.Lys970Arg
XM_011519025.1:c.2885A>G	XP_011517327.1:p.Lys962Arg
XM_011519026.1:c.2843A>G	XP_011517328.1:p.Lys948Arg
XM_011519029.1:c.1409A>G	XP_011517331.1:p.Lys470Arg
XM_011519030.1:c.761A>G	XP_011517332.1:p.Lys254Arg
XM_011519031.1:c.548A>G	XP_011517333.1:p.Lys183Arg
XM_011519032.1:c.548A>G	XP_011517334.1:p.Lys183Arg
XM_011519033.1:c.2822A>G	XP_011517335.1:p.Lys941Arg
NM_001354263.1:c.2957A>G	NP_001341192.1:p.Lys986Arg
XM_005266105.5:c.2969A>G	XP_005266162.1:p.Lys990Arg
XM_011519021.3:c.2987A>G	XP_011517323.1:p.Lys996Arg
XM_011519022.3:c.2984A>G	XP_011517324.1:p.Lys995Arg
XM_011519023.3:c.2966A>G	XP_011517325.1:p.Lys989Arg
XM_011519029.3:c.1409A>G	XP_011517331.1:p.Lys470Arg
XM_011519030.3:c.761A>G	XP_011517332.1:p.Lys254Arg
XM_017015134.1:c.2963A>G	XP_016870623.1:p.Lys988Arg
XM_017015136.2:c.2879A>G	XP_016870625.1:p.Lys960Arg
XM_017015137.1:c.2864A>G	XP_016870626.1:p.Lys955Arg
XM_017015138.1:c.2864A>G	XP_016870627.1:p.Lys955Arg
XM_024447674.1:c.2807A>G	XP_024303442.1:p.Lys936Arg
XM_024447675.1:c.2741A>G	XP_024303443.1:p.Lys914Arg
XM_024447676.1:c.2102A>G	XP_024303444.1:p.Lys701Arg
XM_024447677.1:c.2102A>G	XP_024303445.1:p.Lys701Arg
XM_024447680.1:c.2720A>G	XP_024303448.1:p.Lys907Arg
NM_024757.5:c.2978A>G MANE Select	NP_079033.4:p.Lys993Arg
NM_001354263.2:c.2957A>G	NP_001341192.1:p.Lys986Arg