Canonical Allele Identifier: CA468161031

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140707479A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137813027A>T , CM000671.2:g.137813027A>T	GRCh38
NC_000009.11:g.140707479A>T , CM000671.1:g.140707479A>T	GRCh37
NC_000009.10:g.139827300A>T	NCBI36
NG_011776.1:g.199036A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.2889A>T MANE Select	ENSP00000417980.1:p.Ser963=
ENST00000636027.1:c.2775A>T	ENSP00000489961.1:p.Ser925=
ENST00000637161.1:c.2796A>T	ENSP00000490328.1:p.Ser932=
ENST00000637261.1:c.2929A>T	ENSP00000490815.1:n.2929A>T
ENST00000637891.1:c.783A>T	ENSP00000490907.1:p.Ser261=
ENST00000460843.5:c.2889A>T	ENSP00000417980.1:p.Ser963=
ENST00000462942.3:c.1746A>T	ENSP00000436107.1:p.Ser582=
ENST00000486164.5:c.576A>T
ENST00000488242.2:n.415A>T
NM_024757.4:c.2889A>T	NP_079033.4:p.Ser963=
XM_005266105.3:c.2880A>T	XP_005266162.1:p.Ser960=
XM_005266110.1:c.2796A>T	XP_005266167.1:p.Ser932=
XM_006717288.2:c.2871A>T	XP_006717351.1:p.Ser957=
XM_011519021.1:c.2898A>T	XP_011517323.1:p.Ser966=
XM_011519022.1:c.2895A>T	XP_011517324.1:p.Ser965=
XM_011519023.1:c.2877A>T	XP_011517325.1:p.Ser959=
XM_011519024.1:c.2820A>T	XP_011517326.1:p.Ser940=
XM_011519025.1:c.2796A>T	XP_011517327.1:p.Ser932=
XM_011519026.1:c.2754A>T	XP_011517328.1:p.Ser918=
XM_011519029.1:c.1320A>T	XP_011517331.1:p.Ser440=
XM_011519030.1:c.672A>T	XP_011517332.1:p.Ser224=
XM_011519031.1:c.459A>T	XP_011517333.1:p.Ser153=
XM_011519032.1:c.459A>T	XP_011517334.1:p.Ser153=
XM_011519033.1:c.2733A>T	XP_011517335.1:p.Ser911=
NM_001354263.1:c.2868A>T	NP_001341192.1:p.Ser956=
XM_005266105.5:c.2880A>T	XP_005266162.1:p.Ser960=
XM_011519021.3:c.2898A>T	XP_011517323.1:p.Ser966=
XM_011519022.3:c.2895A>T	XP_011517324.1:p.Ser965=
XM_011519023.3:c.2877A>T	XP_011517325.1:p.Ser959=
XM_011519029.3:c.1320A>T	XP_011517331.1:p.Ser440=
XM_011519030.3:c.672A>T	XP_011517332.1:p.Ser224=
XM_017015134.1:c.2874A>T	XP_016870623.1:p.Ser958=
XM_017015136.2:c.2790A>T	XP_016870625.1:p.Ser930=
XM_017015137.1:c.2775A>T	XP_016870626.1:p.Ser925=
XM_017015138.1:c.2775A>T	XP_016870627.1:p.Ser925=
XM_024447674.1:c.2718A>T	XP_024303442.1:p.Ser906=
XM_024447675.1:c.2652A>T	XP_024303443.1:p.Ser884=
XM_024447676.1:c.2013A>T	XP_024303444.1:p.Ser671=
XM_024447677.1:c.2013A>T	XP_024303445.1:p.Ser671=
XM_024447680.1:c.2631A>T	XP_024303448.1:p.Ser877=
NM_024757.5:c.2889A>T MANE Select	NP_079033.4:p.Ser963=
NM_001354263.2:c.2868A>T	NP_001341192.1:p.Ser956=