Canonical Allele Identifier: CA468161027

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140707473G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137813021G>T , CM000671.2:g.137813021G>T	GRCh38
NC_000009.11:g.140707473G>T , CM000671.1:g.140707473G>T	GRCh37
NC_000009.10:g.139827294G>T	NCBI36
NG_011776.1:g.199030G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.2883G>T MANE Select	ENSP00000417980.1:p.Arg961=
ENST00000636027.1:c.2769G>T	ENSP00000489961.1:p.Arg923=
ENST00000637161.1:c.2790G>T	ENSP00000490328.1:p.Arg930=
ENST00000637261.1:c.2923G>T	ENSP00000490815.1:n.2923G>T
ENST00000637891.1:c.777G>T	ENSP00000490907.1:p.Arg259=
ENST00000460843.5:c.2883G>T	ENSP00000417980.1:p.Arg961=
ENST00000462942.3:c.1740G>T	ENSP00000436107.1:p.Arg580=
ENST00000486164.5:c.570G>T
ENST00000488242.2:n.409G>T
NM_024757.4:c.2883G>T	NP_079033.4:p.Arg961=
XM_005266105.3:c.2874G>T	XP_005266162.1:p.Arg958=
XM_005266110.1:c.2790G>T	XP_005266167.1:p.Arg930=
XM_006717288.2:c.2865G>T	XP_006717351.1:p.Arg955=
XM_011519021.1:c.2892G>T	XP_011517323.1:p.Arg964=
XM_011519022.1:c.2889G>T	XP_011517324.1:p.Arg963=
XM_011519023.1:c.2871G>T	XP_011517325.1:p.Arg957=
XM_011519024.1:c.2814G>T	XP_011517326.1:p.Arg938=
XM_011519025.1:c.2790G>T	XP_011517327.1:p.Arg930=
XM_011519026.1:c.2748G>T	XP_011517328.1:p.Arg916=
XM_011519029.1:c.1314G>T	XP_011517331.1:p.Arg438=
XM_011519030.1:c.666G>T	XP_011517332.1:p.Arg222=
XM_011519031.1:c.453G>T	XP_011517333.1:p.Arg151=
XM_011519032.1:c.453G>T	XP_011517334.1:p.Arg151=
XM_011519033.1:c.2727G>T	XP_011517335.1:p.Arg909=
NM_001354263.1:c.2862G>T	NP_001341192.1:p.Arg954=
XM_005266105.5:c.2874G>T	XP_005266162.1:p.Arg958=
XM_011519021.3:c.2892G>T	XP_011517323.1:p.Arg964=
XM_011519022.3:c.2889G>T	XP_011517324.1:p.Arg963=
XM_011519023.3:c.2871G>T	XP_011517325.1:p.Arg957=
XM_011519029.3:c.1314G>T	XP_011517331.1:p.Arg438=
XM_011519030.3:c.666G>T	XP_011517332.1:p.Arg222=
XM_017015134.1:c.2868G>T	XP_016870623.1:p.Arg956=
XM_017015136.2:c.2784G>T	XP_016870625.1:p.Arg928=
XM_017015137.1:c.2769G>T	XP_016870626.1:p.Arg923=
XM_017015138.1:c.2769G>T	XP_016870627.1:p.Arg923=
XM_024447674.1:c.2712G>T	XP_024303442.1:p.Arg904=
XM_024447675.1:c.2646G>T	XP_024303443.1:p.Arg882=
XM_024447676.1:c.2007G>T	XP_024303444.1:p.Arg669=
XM_024447677.1:c.2007G>T	XP_024303445.1:p.Arg669=
XM_024447680.1:c.2625G>T	XP_024303448.1:p.Arg875=
NM_024757.5:c.2883G>T MANE Select	NP_079033.4:p.Arg961=
NM_001354263.2:c.2862G>T	NP_001341192.1:p.Arg954=